We will be switching to the new UniProt website soon. Please explore and share your feedback.
Take me to the new website.
UniProtKB - Q9UJV3 (TRIM1_HUMAN)
Protein
Probable E3 ubiquitin-protein ligase MID2
Gene
MID2
Organism
Homo sapiens (Human)
Status
Functioni
May play a role in microtubule stabilization.
1 PublicationCaution
It is uncertain whether Met-1 or Met-21 is the initiator.Curated
Catalytic activityi
- S-ubiquitinyl-[E2 ubiquitin-conjugating enzyme]-L-cysteine + [acceptor protein]-L-lysine = [E2 ubiquitin-conjugating enzyme]-L-cysteine + N(6)-ubiquitinyl-[acceptor protein]-L-lysine. EC:2.3.2.27
: protein ubiquitination Pathwayi
This protein is involved in the pathway protein ubiquitination, which is part of Protein modification.View all proteins of this organism that are known to be involved in the pathway protein ubiquitination and in Protein modification.
Sites
Feature key | Position(s) | DescriptionActions | Graphical view | Length |
---|---|---|---|---|
Metal bindingi | 195 | ZincPROSITE-ProRule annotation | 1 | |
Metal bindingi | 198 | ZincPROSITE-ProRule annotation | 1 | |
Metal bindingi | 218 | ZincPROSITE-ProRule annotation | 1 | |
Metal bindingi | 224 | ZincPROSITE-ProRule annotation | 1 |
Regions
Feature key | Position(s) | DescriptionActions | Graphical view | Length |
---|---|---|---|---|
Zinc fingeri | 30 – 80 | RING-typePROSITE-ProRule annotationAdd BLAST | 51 | |
Zinc fingeri | 137 – 184 | B box-type 1; degeneratePROSITE-ProRule annotationAdd BLAST | 48 | |
Zinc fingeri | 190 – 232 | B box-type 2PROSITE-ProRule annotationAdd BLAST | 43 |
GO - Molecular functioni
- enzyme binding Source: UniProtKB
- identical protein binding Source: IntAct
- microtubule binding Source: UniProtKB
- phosphoprotein binding Source: UniProtKB
- protein homodimerization activity Source: UniProtKB
- transcription coactivator activity Source: ARUK-UCL
- transferase activity Source: UniProtKB-KW
- zinc ion binding Source: InterPro
GO - Biological processi
- innate immune response Source: UniProtKB
- negative regulation of viral entry into host cell Source: UniProtKB
- negative regulation of viral transcription Source: UniProtKB
- positive regulation of autophagy Source: UniProtKB
- positive regulation of DNA-binding transcription factor activity Source: UniProtKB
- positive regulation of I-kappaB kinase/NF-kappaB signaling Source: UniProtKB
- positive regulation of NF-kappaB transcription factor activity Source: UniProtKB
- protein localization to microtubule Source: UniProtKB
- protein ubiquitination Source: UniProtKB-UniPathway
- suppression of viral release by host Source: UniProtKB
Keywordsi
Molecular function | Transferase |
Biological process | Ubl conjugation pathway |
Ligand | Metal-binding, Zinc |
Enzyme and pathway databases
PathwayCommonsi | Q9UJV3 |
SignaLinki | Q9UJV3 |
UniPathwayi | UPA00143 |
Protein family/group databases
MoonDBi | Q9UJV3, Predicted |
Names & Taxonomyi
Protein namesi | Recommended name: Probable E3 ubiquitin-protein ligase MID2 (EC:2.3.2.27)Alternative name(s): Midin-2 Midline defect 2 Midline-2 RING finger protein 60 RING-type E3 ubiquitin transferase MID2Curated Tripartite motif-containing protein 1 |
Gene namesi | Name:MID2 Synonyms:FXY2, RNF60, TRIM1 |
Organismi | Homo sapiens (Human) |
Taxonomic identifieri | 9606 [NCBI] |
Taxonomic lineagei | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo |
Proteomesi |
|
Organism-specific databases
HGNCi | HGNC:7096, MID2 |
MIMi | 300204, gene |
neXtProti | NX_Q9UJV3 |
VEuPathDBi | HostDB:ENSG00000080561 |
Subcellular locationi
Cytoplasm and Cytosol
Cytoskeleton
Note: Microtubule-associated.
Cytoskeleton
- microtubule Source: UniProtKB
Extracellular region or secreted
- extracellular exosome Source: UniProtKB
Other locations
- cytoplasm Source: UniProtKB-SubCell
Keywords - Cellular componenti
Cytoplasm, Cytoskeleton, MicrotubulePathology & Biotechi
Involvement in diseasei
Intellectual developmental disorder, X-linked 101 (XLID101)1 Publication
The disease is caused by variants affecting the gene represented in this entry.
Disease descriptionA disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. Intellectual deficiency is the only primary symptom of non-syndromic X-linked mental retardation, while syndromic mental retardation presents with associated physical, neurological and/or psychiatric manifestations. XLID101 clinical features include global developmental delay, hyperactivity often with aggressive outbursts, and seizures in some patients. Several affected individuals have long face, prominent ears, and squint or strabismus.
Related information in OMIMFeature key | Position(s) | DescriptionActions | Graphical view | Length |
---|---|---|---|---|
Natural variantiVAR_071836 | 347 | R → Q in XLID101; the mutant is abnormally localized in aggregates or enclosed in cytoplasmic vesicles rather than being bound to microtubules. 1 PublicationCorresponds to variant dbSNP:rs587777605EnsemblClinVar. | 1 |
Keywords - Diseasei
Disease variant, Mental retardationOrganism-specific databases
DisGeNETi | 11043 |
MalaCardsi | MID2 |
MIMi | 300928, phenotype |
OpenTargetsi | ENSG00000080561 |
Orphaneti | 777, X-linked non-syndromic intellectual disability |
PharmGKBi | PA30817 |
Miscellaneous databases
Pharosi | Q9UJV3, Tbio |
Genetic variation databases
BioMutai | MID2 |
DMDMi | 294862489 |
PTM / Processingi
Molecule processing
Feature key | Position(s) | DescriptionActions | Graphical view | Length |
---|---|---|---|---|
ChainiPRO_0000056193 | 1 – 735 | Probable E3 ubiquitin-protein ligase MID2Add BLAST | 735 |
Post-translational modificationi
Phosphorylated on serine and threonine residues.1 Publication
Keywords - PTMi
PhosphoproteinProteomic databases
EPDi | Q9UJV3 |
jPOSTi | Q9UJV3 |
MassIVEi | Q9UJV3 |
MaxQBi | Q9UJV3 |
PaxDbi | Q9UJV3 |
PeptideAtlasi | Q9UJV3 |
PRIDEi | Q9UJV3 |
ProteomicsDBi | 84662 [Q9UJV3-1] 84663 [Q9UJV3-2] |
PTM databases
iPTMneti | Q9UJV3 |
PhosphoSitePlusi | Q9UJV3 |
Expressioni
Tissue specificityi
Low level in fetal kidney and lung, and in adult prostate, ovary and small intestine.
Gene expression databases
Bgeei | ENSG00000080561, Expressed in stomach and 192 other tissues |
ExpressionAtlasi | Q9UJV3, baseline and differential |
Genevisiblei | Q9UJV3, HS |
Organism-specific databases
HPAi | ENSG00000080561, Low tissue specificity |
Interactioni
Subunit structurei
Homodimer or heterodimer with MID1.
Interacts with IGBP1.
1 PublicationBinary interactionsi
MID2 - isoform 2 [Q9UJV3-2]
GO - Molecular functioni
- enzyme binding Source: UniProtKB
- identical protein binding Source: IntAct
- microtubule binding Source: UniProtKB
- phosphoprotein binding Source: UniProtKB
- protein homodimerization activity Source: UniProtKB
Protein-protein interaction databases
BioGRIDi | 116231, 279 interactors |
IntActi | Q9UJV3, 252 interactors |
MINTi | Q9UJV3 |
STRINGi | 9606.ENSP00000262843 |
Miscellaneous databases
RNActi | Q9UJV3, protein |
Structurei
Secondary structure
Legend: HelixTurnBeta strandPDB Structure known for this area
Show more details3D structure databases
BMRBi | Q9UJV3 |
SMRi | Q9UJV3 |
ModBasei | Search... |
PDBe-KBi | Search... |
Miscellaneous databases
EvolutionaryTracei | Q9UJV3 |
Family & Domainsi
Domains and Repeats
Feature key | Position(s) | DescriptionActions | Graphical view | Length |
---|---|---|---|---|
Domaini | 340 – 399 | COSPROSITE-ProRule annotationAdd BLAST | 60 | |
Domaini | 398 – 531 | Fibronectin type-IIIAdd BLAST | 134 | |
Domaini | 516 – 709 | B30.2/SPRYPROSITE-ProRule annotationAdd BLAST | 194 |
Coiled coil
Feature key | Position(s) | DescriptionActions | Graphical view | Length |
---|---|---|---|---|
Coiled coili | 233 – 301 | Sequence analysisAdd BLAST | 69 |
Domaini
The tripartite motif (RBCC; RING- and B box-type zinc fingers and coiled coil domains) mediates dimerization.By similarity
Associates with microtubules in a manner that is dependent on the C-terminal B30.2 domain.
Sequence similaritiesi
Belongs to the TRIM/RBCC family.Curated
Zinc finger
Feature key | Position(s) | DescriptionActions | Graphical view | Length |
---|---|---|---|---|
Zinc fingeri | 30 – 80 | RING-typePROSITE-ProRule annotationAdd BLAST | 51 | |
Zinc fingeri | 137 – 184 | B box-type 1; degeneratePROSITE-ProRule annotationAdd BLAST | 48 | |
Zinc fingeri | 190 – 232 | B box-type 2PROSITE-ProRule annotationAdd BLAST | 43 |
Keywords - Domaini
Coiled coil, Repeat, Zinc-fingerPhylogenomic databases
eggNOGi | KOG2177, Eukaryota |
GeneTreei | ENSGT00940000159460 |
HOGENOMi | CLU_013137_19_4_1 |
InParanoidi | Q9UJV3 |
OMAi | GERIACQ |
OrthoDBi | 172471at2759 |
PhylomeDBi | Q9UJV3 |
TreeFami | TF333654 |
Family and domain databases
CDDi | cd00063, FN3, 1 hit cd13739, SPRY_PRY_TRIM1, 1 hit |
Gene3Di | 2.60.120.920, 1 hit 2.60.40.10, 1 hit 3.30.40.10, 1 hit |
InterProi | View protein in InterPro IPR001870, B30.2/SPRY IPR043136, B30.2/SPRY_sf IPR003649, Bbox_C IPR003879, Butyrophylin_SPRY IPR013320, ConA-like_dom_sf IPR017903, COS_domain IPR003961, FN3_dom IPR036116, FN3_sf IPR013783, Ig-like_fold IPR033491, MID2 IPR040859, Midline-1_COS IPR035752, SPRY/PRY_TRIM1 IPR003877, SPRY_dom IPR027370, Znf-RING_LisH IPR000315, Znf_B-box IPR001841, Znf_RING IPR013083, Znf_RING/FYVE/PHD IPR017907, Znf_RING_CS |
PANTHERi | PTHR24099:SF12, PTHR24099:SF12, 1 hit |
Pfami | View protein in Pfam PF18568, COS, 1 hit PF00622, SPRY, 1 hit PF00643, zf-B_box, 1 hit PF13445, zf-RING_UBOX, 1 hit |
PRINTSi | PR01407, BUTYPHLNCDUF |
SMARTi | View protein in SMART SM00502, BBC, 1 hit SM00336, BBOX, 2 hits SM00060, FN3, 1 hit SM00184, RING, 1 hit SM00449, SPRY, 1 hit |
SUPFAMi | SSF49265, SSF49265, 1 hit SSF49899, SSF49899, 1 hit |
PROSITEi | View protein in PROSITE PS50188, B302_SPRY, 1 hit PS51262, COS, 1 hit PS50119, ZF_BBOX, 1 hit PS00518, ZF_RING_1, 1 hit PS50089, ZF_RING_2, 1 hit |
s (2+)i Sequence
Sequence statusi: Complete.
This entry describes 2 produced by isoformsialternative splicing. AlignAdd to basketThis entry has 2 described isoforms and 1 potential isoform that is computationally mapped.Show allAlign All
Isoform 1 (identifier: Q9UJV3-1) [UniParc]FASTAAdd to basket
This isoform has been chosen as the sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry. canonicali
10 20 30 40 50
MGESPASVVL NASGGLFSLK METLESELTC PICLELFEDP LLLPCAHSLC
60 70 80 90 100
FSCAHRILVS SCSSGESIEP ITAFQCPTCR YVISLNHRGL DGLKRNVTLQ
110 120 130 140 150
NIIDRFQKAS VSGPNSPSES RRERTYRPTT AMSSERIACQ FCEQDPPRDA
160 170 180 190 200
VKTCITCEVS YCDRCLRATH PNKKPFTSHR LVEPVPDTHL RGITCLDHEN
210 220 230 240 250
EKVNMYCVSD DQLICALCKL VGRHRDHQVA SLNDRFEKLK QTLEMNLTNL
260 270 280 290 300
VKRNSELENQ MAKLIQICQQ VEVNTAMHEA KLMEECDELV EIIQQRKQMI
310 320 330 340 350
AVKIKETKVM KLRKLAQQVA NCRQCLERST VLINQAEHIL KENDQARFLQ
360 370 380 390 400
SAKNIAERVA MATASSQVLI PDINFNDAFE NFALDFSREK KLLEGLDYLT
410 420 430 440 450
APNPPSIREE LCTASHDTIT VHWISDDEFS ISSYELQYTI FTGQANFISK
460 470 480 490 500
SWCSWGLWPE IRKCKEAVSC SRLAGAPRGL YNSVDSWMIV PNIKQNHYTV
510 520 530 540 550
HGLQSGTRYI FIVKAINQAG SRNSEPTRLK TNSQPFKLDP KMTHKKLKIS
560 570 580 590 600
NDGLQMEKDE SSLKKSHTPE RFSGTGCYGA AGNIFIDSGC HYWEVVMGSS
610 620 630 640 650
TWYAIGIAYK SAPKNEWIGK NASSWVFSRC NSNFVVRHNN KEMLVDVPPH
660 670 680 690 700
LKRLGVLLDY DNNMLSFYDP ANSLHLHTFD VTFILPVCPT FTIWNKSLMI
710 720 730
LSGLPAPDFI DYPERQECNC RPQESPYVSG MKTCH
Computationally mapped potential isoform sequencesi
There is 1 potential isoform mapped to this entry.BLASTAlignShow allAdd to basketA6PVI4 | A6PVI4_HUMAN | Probable E3 ubiquitin-protein ligas... | MID2 | 218 | Annotation score: |
Sequence cautioni
The sequence AAF07341 differs from that shown. Reason: Erroneous initiation. Truncated N-terminus.Curated
The sequence AAH17707 differs from that shown. Reason: Erroneous initiation. Truncated N-terminus.Curated
The sequence CAB56154 differs from that shown. Reason: Erroneous initiation. Truncated N-terminus.Curated
Natural variant
Feature key | Position(s) | DescriptionActions | Graphical view | Length |
---|---|---|---|---|
Natural variantiVAR_071835 | 343 | N → S The protein is normally bound to microtubules. 1 PublicationCorresponds to variant dbSNP:rs551253128EnsemblClinVar. | 1 | |
Natural variantiVAR_071836 | 347 | R → Q in XLID101; the mutant is abnormally localized in aggregates or enclosed in cytoplasmic vesicles rather than being bound to microtubules. 1 PublicationCorresponds to variant dbSNP:rs587777605EnsemblClinVar. | 1 | |
Natural variantiVAR_052123 | 378 | A → D. Corresponds to variant dbSNP:rs12849510Ensembl. | 1 |
Alternative sequence
Feature key | Position(s) | DescriptionActions | Graphical view | Length |
---|---|---|---|---|
Alternative sequenceiVSP_009009 | 450 – 479 | Missing in isoform 2. 3 PublicationsAdd BLAST | 30 |
Sequence databases
Select the link destinations: EMBLi GenBanki DDBJi Links Updated | AF196481 mRNA Translation: AAF07341.1 Different initiation. Y18880 mRNA Translation: CAB56154.1 Different initiation. AL034399 Genomic DNA No translation available. AL109946 Genomic DNA No translation available. BC017707 mRNA Translation: AAH17707.1 Different initiation. BT006663 mRNA Translation: AAP35309.1 |
CCDSi | CCDS14532.2 [Q9UJV3-1] CCDS14533.2 [Q9UJV3-2] |
RefSeqi | NP_036348.2, NM_012216.3 [Q9UJV3-1] NP_438112.2, NM_052817.2 [Q9UJV3-2] XP_005262119.1, XM_005262062.4 XP_016884728.1, XM_017029239.1 |
Genome annotation databases
Ensembli | ENST00000262843; ENSP00000262843; ENSG00000080561 ENST00000443968; ENSP00000413976; ENSG00000080561 [Q9UJV3-2] |
GeneIDi | 11043 |
KEGGi | hsa:11043 |
MANE-Selecti | ENST00000262843.11; ENSP00000262843.6; NM_012216.4; NP_036348.2 |
UCSCi | uc004enk.4, human [Q9UJV3-1] |
Keywords - Coding sequence diversityi
Alternative splicingSimilar proteinsi
Cross-referencesi
Sequence databases
Select the link destinations: EMBLi GenBanki DDBJi Links Updated | AF196481 mRNA Translation: AAF07341.1 Different initiation. Y18880 mRNA Translation: CAB56154.1 Different initiation. AL034399 Genomic DNA No translation available. AL109946 Genomic DNA No translation available. BC017707 mRNA Translation: AAH17707.1 Different initiation. BT006663 mRNA Translation: AAP35309.1 |
CCDSi | CCDS14532.2 [Q9UJV3-1] CCDS14533.2 [Q9UJV3-2] |
RefSeqi | NP_036348.2, NM_012216.3 [Q9UJV3-1] NP_438112.2, NM_052817.2 [Q9UJV3-2] XP_005262119.1, XM_005262062.4 XP_016884728.1, XM_017029239.1 |
3D structure databases
Select the link destinations: PDBei RCSB PDBi PDBji Links Updated | PDB entry | Method | Resolution (Å) | Chain | Positions | PDBsum |
2DJA | NMR | - | A | 182-252 | [»] | |
2DMK | NMR | - | A | 394-537 | [»] | |
BMRBi | Q9UJV3 | |||||
SMRi | Q9UJV3 | |||||
ModBasei | Search... | |||||
PDBe-KBi | Search... |
Protein-protein interaction databases
BioGRIDi | 116231, 279 interactors |
IntActi | Q9UJV3, 252 interactors |
MINTi | Q9UJV3 |
STRINGi | 9606.ENSP00000262843 |
Protein family/group databases
MoonDBi | Q9UJV3, Predicted |
PTM databases
iPTMneti | Q9UJV3 |
PhosphoSitePlusi | Q9UJV3 |
Genetic variation databases
BioMutai | MID2 |
DMDMi | 294862489 |
Proteomic databases
EPDi | Q9UJV3 |
jPOSTi | Q9UJV3 |
MassIVEi | Q9UJV3 |
MaxQBi | Q9UJV3 |
PaxDbi | Q9UJV3 |
PeptideAtlasi | Q9UJV3 |
PRIDEi | Q9UJV3 |
ProteomicsDBi | 84662 [Q9UJV3-1] 84663 [Q9UJV3-2] |
Protocols and materials databases
Antibodypediai | 29334, 185 antibodies from 26 providers |
DNASUi | 11043 |
Genome annotation databases
Ensembli | ENST00000262843; ENSP00000262843; ENSG00000080561 ENST00000443968; ENSP00000413976; ENSG00000080561 [Q9UJV3-2] |
GeneIDi | 11043 |
KEGGi | hsa:11043 |
MANE-Selecti | ENST00000262843.11; ENSP00000262843.6; NM_012216.4; NP_036348.2 |
UCSCi | uc004enk.4, human [Q9UJV3-1] |
Organism-specific databases
CTDi | 11043 |
DisGeNETi | 11043 |
GeneCardsi | MID2 |
HGNCi | HGNC:7096, MID2 |
HPAi | ENSG00000080561, Low tissue specificity |
MalaCardsi | MID2 |
MIMi | 300204, gene 300928, phenotype |
neXtProti | NX_Q9UJV3 |
OpenTargetsi | ENSG00000080561 |
Orphaneti | 777, X-linked non-syndromic intellectual disability |
PharmGKBi | PA30817 |
VEuPathDBi | HostDB:ENSG00000080561 |
GenAtlasi | Search... |
Phylogenomic databases
eggNOGi | KOG2177, Eukaryota |
GeneTreei | ENSGT00940000159460 |
HOGENOMi | CLU_013137_19_4_1 |
InParanoidi | Q9UJV3 |
OMAi | GERIACQ |
OrthoDBi | 172471at2759 |
PhylomeDBi | Q9UJV3 |
TreeFami | TF333654 |
Enzyme and pathway databases
UniPathwayi | UPA00143 |
PathwayCommonsi | Q9UJV3 |
SignaLinki | Q9UJV3 |
Miscellaneous databases
BioGRID-ORCSi | 11043, 3 hits in 704 CRISPR screens |
ChiTaRSi | MID2, human |
EvolutionaryTracei | Q9UJV3 |
GeneWikii | MID2 |
GenomeRNAii | 11043 |
Pharosi | Q9UJV3, Tbio |
PROi | PR:Q9UJV3 |
RNActi | Q9UJV3, protein |
SOURCEi | Search... |
Gene expression databases
Bgeei | ENSG00000080561, Expressed in stomach and 192 other tissues |
ExpressionAtlasi | Q9UJV3, baseline and differential |
Genevisiblei | Q9UJV3, HS |
Family and domain databases
CDDi | cd00063, FN3, 1 hit cd13739, SPRY_PRY_TRIM1, 1 hit |
Gene3Di | 2.60.120.920, 1 hit 2.60.40.10, 1 hit 3.30.40.10, 1 hit |
InterProi | View protein in InterPro IPR001870, B30.2/SPRY IPR043136, B30.2/SPRY_sf IPR003649, Bbox_C IPR003879, Butyrophylin_SPRY IPR013320, ConA-like_dom_sf IPR017903, COS_domain IPR003961, FN3_dom IPR036116, FN3_sf IPR013783, Ig-like_fold IPR033491, MID2 IPR040859, Midline-1_COS IPR035752, SPRY/PRY_TRIM1 IPR003877, SPRY_dom IPR027370, Znf-RING_LisH IPR000315, Znf_B-box IPR001841, Znf_RING IPR013083, Znf_RING/FYVE/PHD IPR017907, Znf_RING_CS |
PANTHERi | PTHR24099:SF12, PTHR24099:SF12, 1 hit |
Pfami | View protein in Pfam PF18568, COS, 1 hit PF00622, SPRY, 1 hit PF00643, zf-B_box, 1 hit PF13445, zf-RING_UBOX, 1 hit |
PRINTSi | PR01407, BUTYPHLNCDUF |
SMARTi | View protein in SMART SM00502, BBC, 1 hit SM00336, BBOX, 2 hits SM00060, FN3, 1 hit SM00184, RING, 1 hit SM00449, SPRY, 1 hit |
SUPFAMi | SSF49265, SSF49265, 1 hit SSF49899, SSF49899, 1 hit |
PROSITEi | View protein in PROSITE PS50188, B302_SPRY, 1 hit PS51262, COS, 1 hit PS50119, ZF_BBOX, 1 hit PS00518, ZF_RING_1, 1 hit PS50089, ZF_RING_2, 1 hit |
MobiDBi | Search... |
Entry informationi
Entry namei | TRIM1_HUMAN | |
Accessioni | Q9UJV3Primary (citable) accession number: Q9UJV3 Secondary accession number(s): A6NEL8 Q9UJR9 | |
Entry historyi | Integrated into UniProtKB/Swiss-Prot: | November 28, 2003 |
Last sequence update: | April 20, 2010 | |
Last modified: | February 23, 2022 | |
This is version 202 of the entry and version 3 of the sequence. See complete history. | ||
Entry statusi | Reviewed (UniProtKB/Swiss-Prot) | |
Annotation program | Chordata Protein Annotation Program | |
Disclaimer | Any 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, Reference proteomeDocuments
- Human chromosome X
Human chromosome X: entries, gene names and cross-references to MIM - Human entries with genetic variants
List of human entries with genetic variants - Human variants curated from literature reports
Index of human variants curated from literature reports - MIM cross-references
Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot - PATHWAY comments
Index of metabolic and biosynthesis pathways - PDB cross-references
Index of Protein Data Bank (PDB) cross-references - SIMILARITY comments
Index of protein domains and families