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Protein

Myosin-14

Gene

MYH14

Organism
Homo sapiens (Human)
Status
Reviewed-Annotation score: Annotation score: 5 out of 5-Experimental evidence at protein leveli

Functioni

Cellular myosin that appears to play a role in cytokinesis, cell shape, and specialized functions such as secretion and capping.By similarity

Regions

Feature keyPosition(s)DescriptionActionsGraphical viewLength
Nucleotide bindingi198 – 205ATPSequence analysis8

GO - Molecular functioni

GO - Biological processi

  • actin filament-based movement Source: Ensembl
  • actomyosin structure organization Source: UniProtKB
  • mitochondrion morphogenesis Source: UniProtKB
  • neuronal action potential Source: UniProtKB
  • regulation of cell shape Source: UniProtKB-KW
  • sensory perception of sound Source: UniProtKB
  • skeletal muscle contraction Source: UniProtKB
  • skeletal muscle tissue development Source: UniProtKB
  • vocalization behavior Source: UniProtKB
Complete GO annotation...

Keywords - Molecular functioni

Motor protein, Myosin

Keywords - Biological processi

Cell shape

Keywords - Ligandi

Actin-binding, ATP-binding, Calmodulin-binding, Nucleotide-binding

Enzyme and pathway databases

ReactomeiR-HSA-3928663. EPHA-mediated growth cone collapse.
R-HSA-416572. Sema4D induced cell migration and growth-cone collapse.
R-HSA-5625740. RHO GTPases activate PKNs.
R-HSA-5625900. RHO GTPases activate CIT.
R-HSA-5627117. RHO GTPases Activate ROCKs.
R-HSA-5627123. RHO GTPases activate PAKs.

Names & Taxonomyi

Protein namesi
Recommended name:
Myosin-14
Alternative name(s):
Myosin heavy chain 14
Myosin heavy chain, non-muscle IIc
Non-muscle myosin heavy chain IIc
Short name:
NMHC II-C
Gene namesi
Name:MYH14
Synonyms:KIAA2034
ORF Names:FP17425
OrganismiHomo sapiens (Human)
Taxonomic identifieri9606 [NCBI]
Taxonomic lineageiEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo
Proteomesi
  • UP000005640 Componenti: Chromosome 19

Organism-specific databases

HGNCiHGNC:23212. MYH14.

Subcellular locationi

GO - Cellular componenti

  • actomyosin Source: UniProtKB
  • axon Source: Ensembl
  • brush border Source: Ensembl
  • cytosol Source: Reactome
  • extracellular exosome Source: UniProtKB
  • growth cone Source: Ensembl
  • membrane Source: UniProtKB
  • myelin sheath Source: Ensembl
  • myosin II complex Source: UniProtKB
  • myosin II filament Source: UniProtKB
  • stress fiber Source: Ensembl
Complete GO annotation...

Pathology & Biotechi

Involvement in diseasei

Deafness, autosomal dominant, 4A (DFNA4A)2 Publications
The disease is caused by mutations affecting the gene represented in this entry.
Disease descriptionA form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information.
See also OMIM:600652
Feature keyPosition(s)DescriptionActionsGraphical viewLength
Natural variantiVAR_037302120S → L in DFNA4A. 1 PublicationCorresponds to variant rs119103281dbSNPEnsembl.1
Natural variantiVAR_022867376G → C in DFNA4A. 1 PublicationCorresponds to variant rs119103280dbSNPEnsembl.1
Natural variantiVAR_022868726R → S in DFNA4A. 1 PublicationCorresponds to variant rs28940307dbSNPEnsembl.1
Natural variantiVAR_022869976L → F in DFNA4A. 1 PublicationCorresponds to variant rs28940306dbSNPEnsembl.1
Peripheral neuropathy, myopathy, hoarseness, and hearing loss (PNMHH)1 Publication
The disease is caused by mutations affecting the gene represented in this entry.
Disease descriptionA complex phenotype of progressive peripheral neuropathy and distal myopathy, with later onset of hoarseness and hearing loss. Affected individuals develop distal muscle weakness at a mean age of 10.6 years, followed by progressive atrophy of these muscles. The lower limbs are more severely affected than the upper limbs, and the muscle weakness first affects anterior leg muscles and later posterior leg muscles.
See also OMIM:614369
Feature keyPosition(s)DescriptionActionsGraphical viewLength
Natural variantiVAR_066338933R → L in PNMHH. 1 PublicationCorresponds to variant rs113993956dbSNPEnsembl.1

Keywords - Diseasei

Deafness, Disease mutation, Neuropathy, Non-syndromic deafness

Organism-specific databases

DisGeNETi79784.
MalaCardsiMYH14.
MIMi600652. phenotype.
614369. phenotype.
OpenTargetsiENSG00000105357.
Orphaneti90635. Autosomal dominant non-syndromic sensorineural deafness type DFNA.
397744. Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome.
PharmGKBiPA134935217.

Polymorphism and mutation databases

BioMutaiMYH14.
DMDMi327478526.

PTM / Processingi

Molecule processing

Feature keyPosition(s)DescriptionActionsGraphical viewLength
Initiator methionineiRemoved1 Publication
ChainiPRO_00001234312 – 1995Myosin-14Add BLAST1994

Amino acid modifications

Feature keyPosition(s)DescriptionActionsGraphical viewLength
Modified residuei2N-acetylalanine1 Publication1
Modified residuei60PhosphoserineCombined sources1
Modified residuei1194PhosphothreonineCombined sources1
Modified residuei1969PhosphoserineCombined sources1
Modified residuei1980PhosphoserineCombined sources1
Modified residuei1983PhosphoserineCombined sources1
Modified residuei1989PhosphoserineCombined sources1

Keywords - PTMi

Acetylation, Phosphoprotein

Proteomic databases

EPDiQ7Z406.
MaxQBiQ7Z406.
PaxDbiQ7Z406.
PeptideAtlasiQ7Z406.
PRIDEiQ7Z406.

PTM databases

iPTMnetiQ7Z406.
PhosphoSitePlusiQ7Z406.
SwissPalmiQ7Z406.

Expressioni

Tissue specificityi

High levels of expression are found in brain (highest in corpus callosum), heart, kidney, liver, lung, small intestine, colon and skeletal muscle. Expression is low in organs composed mainly of smooth muscle, such as aorta, uterus and urinary bladder. No detectable expression is found in thymus, spleen, placenta and lymphocytes.3 Publications

Gene expression databases

BgeeiENSG00000105357.
ExpressionAtlasiQ7Z406. baseline and differential.
GenevisibleiQ7Z406. HS.

Organism-specific databases

HPAiHPA067889.
HPA070260.

Interactioni

Subunit structurei

Myosin is a hexameric protein that consists of 2 heavy chain subunits (MHC), 2 alkali light chain subunits (MLC) and 2 regulatory light chain subunits (MLC-2).By similarity

Protein-protein interaction databases

BioGridi122884. 43 interactors.
DIPiDIP-33170N.
IntActiQ7Z406. 23 interactors.
MINTiMINT-1146777.
STRINGi9606.ENSP00000262269.

Structurei

3D structure databases

Select the link destinations:
PDBei
RCSB PDBi
PDBji
Links Updated
PDB entryMethodResolution (Å)ChainPositionsPDBsum
5JLHelectron microscopy3.90F/G1-799[»]
ProteinModelPortaliQ7Z406.
SMRiQ7Z406.
ModBaseiSearch...
MobiDBiSearch...

Family & Domainsi

Domains and Repeats

Feature keyPosition(s)DescriptionActionsGraphical viewLength
Domaini105 – 800Myosin motorAdd BLAST696
Domaini803 – 832IQPROSITE-ProRule annotationAdd BLAST30

Coiled coil

Feature keyPosition(s)DescriptionActionsGraphical viewLength
Coiled coili862 – 1947Sequence analysisAdd BLAST1086

Domaini

The rodlike tail sequence is highly repetitive, showing cycles of a 28-residue repeat pattern composed of 4 heptapeptides, characteristic for alpha-helical coiled coils.By similarity

Sequence similaritiesi

Contains 1 IQ domain.PROSITE-ProRule annotation
Contains 1 myosin motor domain.Curated

Keywords - Domaini

Coiled coil

Phylogenomic databases

eggNOGiKOG0161. Eukaryota.
COG5022. LUCA.
GeneTreeiENSGT00760000118919.
HOVERGENiHBG004704.
InParanoidiQ7Z406.
KOiK10352.
OMAiQDRDEMA.
OrthoDBiEOG091G009J.
PhylomeDBiQ7Z406.
TreeFamiTF333601.

Family and domain databases

Gene3Di4.10.270.10. 1 hit.
InterProiIPR000048. IQ_motif_EF-hand-BS.
IPR027401. Myosin-like_IQ_dom.
IPR001609. Myosin_head_motor_dom.
IPR004009. Myosin_N.
IPR002928. Myosin_tail.
IPR027417. P-loop_NTPase.
[Graphical view]
PfamiPF00063. Myosin_head. 1 hit.
PF02736. Myosin_N. 1 hit.
PF01576. Myosin_tail_1. 1 hit.
[Graphical view]
PRINTSiPR00193. MYOSINHEAVY.
SMARTiSM00015. IQ. 1 hit.
SM00242. MYSc. 1 hit.
[Graphical view]
SUPFAMiSSF52540. SSF52540. 1 hit.
PROSITEiPS50096. IQ. 1 hit.
PS51456. MYOSIN_MOTOR. 1 hit.
[Graphical view]

Sequences (5)i

Sequence statusi: Complete.

Sequence processingi: The displayed sequence is further processed into a mature form.

This entry describes 5 isoformsi produced by alternative splicing. AlignAdd to basket

Isoform 1 (identifier: Q7Z406-1) [UniParc]FASTAAdd to basket

This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry.

« Hide

        10         20         30         40         50
MAAVTMSVPG RKAPPRPGPV PEAAQPFLFT PRGPSAGGGP GSGTSPQVEW
60 70 80 90 100
TARRLVWVPS ELHGFEAAAL RDEGEEEAEV ELAESGRRLR LPRDQIQRMN
110 120 130 140 150
PPKFSKAEDM AELTCLNEAS VLHNLRERYY SGLIYTYSGL FCVVINPYKQ
160 170 180 190 200
LPIYTEAIVE MYRGKKRHEV PPHVYAVTEG AYRSMLQDRE DQSILCTGES
210 220 230 240 250
GAGKTENTKK VIQYLAHVAS SPKGRKEPGV PGELERQLLQ ANPILEAFGN
260 270 280 290 300
AKTVKNDNSS RFGKFIRINF DVAGYIVGAN IETYLLEKSR AIRQAKDECS
310 320 330 340 350
FHIFYQLLGG AGEQLKADLL LEPCSHYRFL TNGPSSSPGQ ERELFQETLE
360 370 380 390 400
SLRVLGFSHE EIISMLRMVS AVLQFGNIAL KRERNTDQAT MPDNTAAQKL
410 420 430 440 450
CRLLGLGVTD FSRALLTPRI KVGRDYVQKA QTKEQADFAL EALAKATYER
460 470 480 490 500
LFRWLVLRLN RALDRSPRQG ASFLGILDIA GFEIFQLNSF EQLCINYTNE
510 520 530 540 550
KLQQLFNHTM FVLEQEEYQR EGIPWTFLDF GLDLQPCIDL IERPANPPGL
560 570 580 590 600
LALLDEECWF PKATDKSFVE KVAQEQGGHP KFQRPRHLRD QADFSVLHYA
610 620 630 640 650
GKVDYKANEW LMKNMDPLND NVAALLHQST DRLTAEIWKD VEGIVGLEQV
660 670 680 690 700
SSLGDGPPGG RPRRGMFRTV GQLYKESLSR LMATLSNTNP SFVRCIVPNH
710 720 730 740 750
EKRAGKLEPR LVLDQLRCNG VLEGIRICRQ GFPNRILFQE FRQRYEILTP
760 770 780 790 800
NAIPKGFMDG KQACEKMIQA LELDPNLYRV GQSKIFFRAG VLAQLEEERD
810 820 830 840 850
LKVTDIIVSF QAAARGYLAR RAFQKRQQQQ SALRVMQRNC AAYLKLRHWQ
860 870 880 890 900
WWRLFTKVKP LLQVTRQDEV LQARAQELQK VQELQQQSAR EVGELQGRVA
910 920 930 940 950
QLEEERARLA EQLRAEAELC AEAEETRGRL AARKQELELV VSELEARVGE
960 970 980 990 1000
EEECSRQMQT EKKRLQQHIQ ELEAHLEAEE GARQKLQLEK VTTEAKMKKF
1010 1020 1030 1040 1050
EEDLLLLEDQ NSKLSKERKL LEDRLAEFSS QAAEEEEKVK SLNKLRLKYE
1060 1070 1080 1090 1100
ATIADMEDRL RKEEKGRQEL EKLKRRLDGE SSELQEQMVE QQQRAEELRA
1110 1120 1130 1140 1150
QLGRKEEELQ AALARAEDEG GARAQLLKSL REAQAALAEA QEDLESERVA
1160 1170 1180 1190 1200
RTKAEKQRRD LGEELEALRG ELEDTLDSTN AQQELRSKRE QEVTELKKTL
1210 1220 1230 1240 1250
EEETRIHEAA VQELRQRHGQ ALGELAEQLE QARRGKGAWE KTRLALEAEV
1260 1270 1280 1290 1300
SELRAELSSL QTARQEGEQR RRRLELQLQE VQGRAGDGER ARAEAAEKLQ
1310 1320 1330 1340 1350
RAQAELENVS GALNEAESKT IRLSKELSST EAQLHDAQEL LQEETRAKLA
1360 1370 1380 1390 1400
LGSRVRAMEA EAAGLREQLE EEAAARERAG RELQTAQAQL SEWRRRQEEE
1410 1420 1430 1440 1450
AGALEAGEEA RRRAAREAEA LTQRLAEKTE TVDRLERGRR RLQQELDDAT
1460 1470 1480 1490 1500
MDLEQQRQLV STLEKKQRKF DQLLAEEKAA VLRAVEERER AEAEGREREA
1510 1520 1530 1540 1550
RALSLTRALE EEQEAREELE RQNRALRAEL EALLSSKDDV GKSVHELERA
1560 1570 1580 1590 1600
CRVAEQAAND LRAQVTELED ELTAAEDAKL RLEVTVQALK TQHERDLQGR
1610 1620 1630 1640 1650
DEAGEERRRQ LAKQLRDAEV ERDEERKQRT LAVAARKKLE GELEELKAQM
1660 1670 1680 1690 1700
ASAGQGKEEA VKQLRKMQAQ MKELWREVEE TRTSREEIFS QNRESEKRLK
1710 1720 1730 1740 1750
GLEAEVLRLQ EELAASDRAR RQAQQDRDEM ADEVANGNLS KAAILEEKRQ
1760 1770 1780 1790 1800
LEGRLGQLEE ELEEEQSNSE LLNDRYRKLL LQVESLTTEL SAERSFSAKA
1810 1820 1830 1840 1850
ESGRQQLERQ IQELRGRLGE EDAGARARHK MTIAALESKL AQAEEQLEQE
1860 1870 1880 1890 1900
TRERILSGKL VRRAEKRLKE VVLQVEEERR VADQLRDQLE KGNLRVKQLK
1910 1920 1930 1940 1950
RQLEEAEEEA SRAQAGRRRL QRELEDVTES AESMNREVTT LRNRLRRGPL
1960 1970 1980 1990
TFTTRTVRQV FRLEEGVASD EEAEEAQPGS GPSPEPEGSP PAHPQ
Length:1,995
Mass (Da):227,871
Last modified:April 5, 2011 - v2
Checksum:iC77AAB26817B773B
GO
Isoform 2 (identifier: Q7Z406-2) [UniParc]FASTAAdd to basket

The sequence of this isoform differs from the canonical sequence as follows:
     231-231: P → PASVSTVSY
     640-640: D → DEHGGFQQFSFLGSFPPSPPGSAERCSSAISPPG

Show »
Length:2,036
Mass (Da):232,011
Checksum:i44C56941E575A56D
GO
Isoform 4 (identifier: Q7Z406-4) [UniParc]FASTAAdd to basket

The sequence of this isoform differs from the canonical sequence as follows:
     1317-1532: Missing.

Show »
Length:1,779
Mass (Da):202,995
Checksum:iCB3D84684472B2A1
GO
Isoform 5 (identifier: Q7Z406-5) [UniParc]FASTAAdd to basket

The sequence of this isoform differs from the canonical sequence as follows:
     1451-1478: MDLEQQRQLVSTLEKKQRKFDQLLAEEK → LSPDALTDGAQPPSSLDPTGPCPRNPAL
     1479-1995: Missing.

Show »
Length:1,478
Mass (Da):167,896
Checksum:i24968D882FF859BD
GO
Isoform 6 (identifier: Q7Z406-6) [UniParc]FASTAAdd to basket

The sequence of this isoform differs from the canonical sequence as follows:
     231-231: P → PASVSTVSY

Show »
Length:2,003
Mass (Da):228,665
Checksum:iA8B40CFA23A27902
GO

Sequence cautioni

The sequence AAO39147 differs from that shown. Reason: Frameshift at positions 1017 and 1057.Curated
The sequence AAP34449 differs from that shown. Reason: Frameshift at positions 1016, 1057, 1490 and 1755.Curated
The sequence AAP34449 differs from that shown. Reason: Erroneous initiation. Translation N-terminally extended.Curated
The sequence BAB14735 differs from that shown. Reason: Erroneous initiation. Translation N-terminally extended.Curated
The sequence BG468611 differs from that shown. Reason: Erroneous termination at position 403. Translated as Leu.Curated

Experimental Info

Feature keyPosition(s)DescriptionActionsGraphical viewLength
Sequence conflicti411F → S in BG468611 (PubMed:15489334).Curated1
Sequence conflicti444A → G in BG468611 (PubMed:15489334).Curated1
Sequence conflicti446A → D in BG468611 (PubMed:15489334).Curated1
Sequence conflicti458R → S in BG468611 (PubMed:15489334).Curated1
Sequence conflicti466S → D in BG468611 (PubMed:15489334).Curated1
Sequence conflicti473F → L in BG468611 (PubMed:15489334).Curated1
Sequence conflicti997M → I in AAH18933 (PubMed:15489334).Curated1

Natural variant

Feature keyPosition(s)DescriptionActionsGraphical viewLength
Natural variantiVAR_037302120S → L in DFNA4A. 1 PublicationCorresponds to variant rs119103281dbSNPEnsembl.1
Natural variantiVAR_022866266I → V.1 PublicationCorresponds to variant rs200424400dbSNPEnsembl.1
Natural variantiVAR_056176334P → A.Corresponds to variant rs34498817dbSNPEnsembl.1
Natural variantiVAR_022867376G → C in DFNA4A. 1 PublicationCorresponds to variant rs119103280dbSNPEnsembl.1
Natural variantiVAR_022868726R → S in DFNA4A. 1 PublicationCorresponds to variant rs28940307dbSNPEnsembl.1
Natural variantiVAR_066338933R → L in PNMHH. 1 PublicationCorresponds to variant rs113993956dbSNPEnsembl.1
Natural variantiVAR_022869976L → F in DFNA4A. 1 PublicationCorresponds to variant rs28940306dbSNPEnsembl.1
Natural variantiVAR_0663391154A → V.1 Publication1
Natural variantiVAR_0561771209A → E.Corresponds to variant rs11669191dbSNPEnsembl.1
Natural variantiVAR_0561781540V → I.Corresponds to variant rs680446dbSNPEnsembl.1
Natural variantiVAR_0228701559N → S.1 PublicationCorresponds to variant rs769482601dbSNPEnsembl.1

Alternative sequence

Feature keyPosition(s)DescriptionActionsGraphical viewLength
Alternative sequenceiVSP_040881231P → PASVSTVSY in isoform 2 and isoform 6. 3 Publications1
Alternative sequenceiVSP_040882640D → DEHGGFQQFSFLGSFPPSPP GSAERCSSAISPPG in isoform 2. 2 Publications1
Alternative sequenceiVSP_0146281317 – 1532Missing in isoform 4. 1 PublicationAdd BLAST216
Alternative sequenceiVSP_0146291451 – 1478MDLEQ…LAEEK → LSPDALTDGAQPPSSLDPTG PCPRNPAL in isoform 5. 1 PublicationAdd BLAST28
Alternative sequenceiVSP_0146301479 – 1995Missing in isoform 5. 1 PublicationAdd BLAST517

Sequence databases

Select the link destinations:
EMBLi
GenBanki
DDBJi
Links Updated
AY165122 mRNA. Translation: AAO39147.1. Frameshift.
AB111886 mRNA. Translation: BAC98374.1.
AB290169 mRNA. Translation: BAG06723.1.
AC008655 Genomic DNA. No translation available.
AC010515 Genomic DNA. No translation available.
AC020906 Genomic DNA. No translation available.
BC000676 mRNA. Translation: AAH00676.2.
BC004396 mRNA. Translation: AAH04396.1.
BC007877 mRNA. Translation: AAH07877.2.
BC018933 mRNA. Translation: AAH18933.2.
FJ041910 mRNA. Translation: ACM78630.1.
BG468611 mRNA. No translation available.
AY203926 mRNA. Translation: AAP34449.1. Sequence problems.
CR936653 mRNA. Translation: CAI56791.1.
AK023943 mRNA. Translation: BAB14735.1. Different initiation.
CCDSiCCDS46151.1. [Q7Z406-6]
CCDS54295.1. [Q7Z406-2]
CCDS59411.1. [Q7Z406-1]
RefSeqiNP_001070654.1. NM_001077186.1. [Q7Z406-6]
NP_001139281.1. NM_001145809.1. [Q7Z406-2]
NP_079005.3. NM_024729.3. [Q7Z406-1]
XP_006723449.1. XM_006723386.3. [Q7Z406-6]
XP_011525625.1. XM_011527323.2. [Q7Z406-6]
UniGeneiHs.467142.

Genome annotation databases

EnsembliENST00000376970; ENSP00000366169; ENSG00000105357. [Q7Z406-1]
ENST00000425460; ENSP00000407879; ENSG00000105357. [Q7Z406-6]
ENST00000596571; ENSP00000472819; ENSG00000105357. [Q7Z406-1]
ENST00000598205; ENSP00000472543; ENSG00000105357. [Q7Z406-6]
ENST00000601313; ENSP00000470298; ENSG00000105357. [Q7Z406-2]
GeneIDi79784.
KEGGihsa:79784.
UCSCiuc002prq.2. human. [Q7Z406-1]

Keywords - Coding sequence diversityi

Alternative splicing, Polymorphism

Cross-referencesi

Sequence databases

Select the link destinations:
EMBLi
GenBanki
DDBJi
Links Updated
AY165122 mRNA. Translation: AAO39147.1. Frameshift.
AB111886 mRNA. Translation: BAC98374.1.
AB290169 mRNA. Translation: BAG06723.1.
AC008655 Genomic DNA. No translation available.
AC010515 Genomic DNA. No translation available.
AC020906 Genomic DNA. No translation available.
BC000676 mRNA. Translation: AAH00676.2.
BC004396 mRNA. Translation: AAH04396.1.
BC007877 mRNA. Translation: AAH07877.2.
BC018933 mRNA. Translation: AAH18933.2.
FJ041910 mRNA. Translation: ACM78630.1.
BG468611 mRNA. No translation available.
AY203926 mRNA. Translation: AAP34449.1. Sequence problems.
CR936653 mRNA. Translation: CAI56791.1.
AK023943 mRNA. Translation: BAB14735.1. Different initiation.
CCDSiCCDS46151.1. [Q7Z406-6]
CCDS54295.1. [Q7Z406-2]
CCDS59411.1. [Q7Z406-1]
RefSeqiNP_001070654.1. NM_001077186.1. [Q7Z406-6]
NP_001139281.1. NM_001145809.1. [Q7Z406-2]
NP_079005.3. NM_024729.3. [Q7Z406-1]
XP_006723449.1. XM_006723386.3. [Q7Z406-6]
XP_011525625.1. XM_011527323.2. [Q7Z406-6]
UniGeneiHs.467142.

3D structure databases

Select the link destinations:
PDBei
RCSB PDBi
PDBji
Links Updated
PDB entryMethodResolution (Å)ChainPositionsPDBsum
5JLHelectron microscopy3.90F/G1-799[»]
ProteinModelPortaliQ7Z406.
SMRiQ7Z406.
ModBaseiSearch...
MobiDBiSearch...

Protein-protein interaction databases

BioGridi122884. 43 interactors.
DIPiDIP-33170N.
IntActiQ7Z406. 23 interactors.
MINTiMINT-1146777.
STRINGi9606.ENSP00000262269.

PTM databases

iPTMnetiQ7Z406.
PhosphoSitePlusiQ7Z406.
SwissPalmiQ7Z406.

Polymorphism and mutation databases

BioMutaiMYH14.
DMDMi327478526.

Proteomic databases

EPDiQ7Z406.
MaxQBiQ7Z406.
PaxDbiQ7Z406.
PeptideAtlasiQ7Z406.
PRIDEiQ7Z406.

Protocols and materials databases

Structural Biology KnowledgebaseSearch...

Genome annotation databases

EnsembliENST00000376970; ENSP00000366169; ENSG00000105357. [Q7Z406-1]
ENST00000425460; ENSP00000407879; ENSG00000105357. [Q7Z406-6]
ENST00000596571; ENSP00000472819; ENSG00000105357. [Q7Z406-1]
ENST00000598205; ENSP00000472543; ENSG00000105357. [Q7Z406-6]
ENST00000601313; ENSP00000470298; ENSG00000105357. [Q7Z406-2]
GeneIDi79784.
KEGGihsa:79784.
UCSCiuc002prq.2. human. [Q7Z406-1]

Organism-specific databases

CTDi79784.
DisGeNETi79784.
GeneCardsiMYH14.
GeneReviewsiMYH14.
H-InvDBHIX0015356.
HGNCiHGNC:23212. MYH14.
HPAiHPA067889.
HPA070260.
MalaCardsiMYH14.
MIMi600652. phenotype.
608568. gene.
614369. phenotype.
neXtProtiNX_Q7Z406.
OpenTargetsiENSG00000105357.
Orphaneti90635. Autosomal dominant non-syndromic sensorineural deafness type DFNA.
397744. Peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome.
PharmGKBiPA134935217.
HUGEiSearch...
GenAtlasiSearch...

Phylogenomic databases

eggNOGiKOG0161. Eukaryota.
COG5022. LUCA.
GeneTreeiENSGT00760000118919.
HOVERGENiHBG004704.
InParanoidiQ7Z406.
KOiK10352.
OMAiQDRDEMA.
OrthoDBiEOG091G009J.
PhylomeDBiQ7Z406.
TreeFamiTF333601.

Enzyme and pathway databases

ReactomeiR-HSA-3928663. EPHA-mediated growth cone collapse.
R-HSA-416572. Sema4D induced cell migration and growth-cone collapse.
R-HSA-5625740. RHO GTPases activate PKNs.
R-HSA-5625900. RHO GTPases activate CIT.
R-HSA-5627117. RHO GTPases Activate ROCKs.
R-HSA-5627123. RHO GTPases activate PAKs.

Miscellaneous databases

ChiTaRSiMYH14. human.
GeneWikiiMYH14.
GenomeRNAii79784.
PROiQ7Z406.
SOURCEiSearch...

Gene expression databases

BgeeiENSG00000105357.
ExpressionAtlasiQ7Z406. baseline and differential.
GenevisibleiQ7Z406. HS.

Family and domain databases

Gene3Di4.10.270.10. 1 hit.
InterProiIPR000048. IQ_motif_EF-hand-BS.
IPR027401. Myosin-like_IQ_dom.
IPR001609. Myosin_head_motor_dom.
IPR004009. Myosin_N.
IPR002928. Myosin_tail.
IPR027417. P-loop_NTPase.
[Graphical view]
PfamiPF00063. Myosin_head. 1 hit.
PF02736. Myosin_N. 1 hit.
PF01576. Myosin_tail_1. 1 hit.
[Graphical view]
PRINTSiPR00193. MYOSINHEAVY.
SMARTiSM00015. IQ. 1 hit.
SM00242. MYSc. 1 hit.
[Graphical view]
SUPFAMiSSF52540. SSF52540. 1 hit.
PROSITEiPS50096. IQ. 1 hit.
PS51456. MYOSIN_MOTOR. 1 hit.
[Graphical view]
ProtoNetiSearch...

Entry informationi

Entry nameiMYH14_HUMAN
AccessioniPrimary (citable) accession number: Q7Z406
Secondary accession number(s): B0I1S2
, C3TTN4, Q5CZ75, Q6XYE4, Q76B62, Q8WV23, Q96I22, Q9BT27, Q9BW35, Q9H882
Entry historyi
Integrated into UniProtKB/Swiss-Prot: July 19, 2005
Last sequence update: April 5, 2011
Last modified: November 2, 2016
This is version 133 of the entry and version 2 of the sequence. [Complete history]
Entry statusiReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
DisclaimerAny medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care.

Miscellaneousi

Keywords - Technical termi

3D-structure, Complete proteome, Direct protein sequencing, Reference proteome

Documents

  1. Human chromosome 19
    Human chromosome 19: entries, gene names and cross-references to MIM
  2. Human entries with polymorphisms or disease mutations
    List of human entries with polymorphisms or disease mutations
  3. Human polymorphisms and disease mutations
    Index of human polymorphisms and disease mutations
  4. MIM cross-references
    Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot
  5. PDB cross-references
    Index of Protein Data Bank (PDB) cross-references
  6. SIMILARITY comments
    Index of protein domains and families

Similar proteinsi

Links to similar proteins from the UniProt Reference Clusters (UniRef) at 100%, 90% and 50% sequence identity:
100%UniRef100 combines identical sequences and sub-fragments with 11 or more residues from any organism into one UniRef entry.
90%UniRef90 is built by clustering UniRef100 sequences that have at least 90% sequence identity to, and 80% overlap with, the longest sequence (a.k.a seed sequence).
50%UniRef50 is built by clustering UniRef90 seed sequences that have at least 50% sequence identity to, and 80% overlap with, the longest sequence in the cluster.