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Q9NV66 (TYW1_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified May 1, 2013. Version 85. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (6) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
tRNA wybutosine-synthesizing protein 1 homolog
Alternative name(s):
Radical S-adenosyl methionine and flavodoxin domain-containing protein 1
tRNA-yW-synthesizing protein
Gene names
Name:TYW1
Synonyms:RSAFD1
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length732 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

General annotation (Comments)

Function

Probable component of the wybutosine biosynthesis pathway. Wybutosine is a hyper modified guanosine with a tricyclic base found at the 3'-position adjacent to the anticodon of eukaryotic phenylalanine tRNA By similarity.

Cofactor

Binds 1 4Fe-4S cluster. The cluster is coordinated with 3 cysteines and an exchangeable S-adenosyl-L-methionine By similarity.

Pathway

tRNA modification; wybutosine-tRNA(Phe) biosynthesis.

Sequence similarities

Belongs to the TYW1 family.

Contains 1 flavodoxin-like domain.

Sequence caution

The sequence AAH15591.1 differs from that shown. Reason: Frameshift at position 663.

The sequence BAB14307.1 differs from that shown. Reason: Erroneous initiation.

Alternative products

This entry describes 2 isoforms produced by alternative splicing. [Align] [Select]
Isoform 1 (identifier: Q9NV66-1)

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.
Isoform 2 (identifier: Q9NV66-2)

The sequence of this isoform differs from the canonical sequence as follows:
     368-384: GYQLIGSHSGVKLCRWT → VHAPRERRLLQTHILWN
     385-732: Missing.
Note: No experimental confirmation available.

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 732732tRNA wybutosine-synthesizing protein 1 homolog
PRO_0000281826

Regions

Domain79 – 237159Flavodoxin-like
Nucleotide binding85 – 895FMN By similarity
Nucleotide binding176 – 20833FMN By similarity

Sites

Metal binding4161Iron-sulfur (4Fe-4S-S-AdoMet) Potential
Metal binding4201Iron-sulfur (4Fe-4S-S-AdoMet) Potential
Metal binding4231Iron-sulfur (4Fe-4S-S-AdoMet) Potential

Natural variations

Alternative sequence368 – 38417GYQLI…LCRWT → VHAPRERRLLQTHILWN in isoform 2.
VSP_024066
Alternative sequence385 – 732348Missing in isoform 2.
VSP_024067
Natural variant4621G → V.
Corresponds to variant rs2261015 [ dbSNP | Ensembl ].
VAR_031288
Natural variant6321H → R. Ref.1
Corresponds to variant rs2949097 [ dbSNP | Ensembl ].
VAR_031289
Natural variant6711D → N. Ref.1
Corresponds to variant rs28450001 [ dbSNP | Ensembl ].
VAR_031290

Experimental info

Sequence conflict3821R → M in BAB14307. Ref.1
Sequence conflict3881L → F in BAB14307. Ref.1
Sequence conflict4161C → Y in BAB14307. Ref.1
Sequence conflict5431K → R in BAB14307. Ref.1

Sequences

Sequence LengthMass (Da)Tools
Isoform 1 [UniParc].

Last modified April 3, 2007. Version 2.
Checksum: 95E8E5C3F88ADD23

FASTA73283,702
        10         20         30         40         50         60 
MDPSADTWDL FSPLISLWIN RFYIYLGFAV SISLWICVQI VIKTQGKNLQ EKSVPKAAQD 

        70         80         90        100        110        120 
LMTNGYVSLQ EKDIFVSGVK IFYGSQTGTA KGFATVLAEA VTSLDLPVAI INLKEYDPDD 

       130        140        150        160        170        180 
HLIEEVTSKN VCVFLVATYT DGLPTESAEW FCKWLEEASI DFRFGKTYLK GMRYAVFGLG 

       190        200        210        220        230        240 
NSAYASHFNK VGKNVDKWLW MLGAHRVMSR GEGDCDVVKS KHGSIEADFR AWKTKFISQL 

       250        260        270        280        290        300 
QALQKGERKK SCGGHCKKGK CESHQHGSEE REEGSHEQDE LHHRDTEEEE PFESSSEEEF 

       310        320        330        340        350        360 
GGEDHQSLNS IVDVEDLGKI MDHVKKEKRE KEQQEEKSGL FRNMGRNEDG ERRAMITPAL 

       370        380        390        400        410        420 
REALTKQGYQ LIGSHSGVKL CRWTKSMLRG RGGCYKHTFY GIESHRCMET TPSLACANKC 

       430        440        450        460        470        480 
VFCWRHHTNP VGTEWRWKMD QPEMILKEAI ENHQNMIKQF KGVPGVKAER FEEGMTVKHC 

       490        500        510        520        530        540 
ALSLVGEPIM YPEINRFLKL LHQCKISSFL VTNAQFPAEI RNLEPVTQLY VSVDASTKDS 

       550        560        570        580        590        600 
LKKIDRPLFK DFWQRFLDSL KALAVKQQRT VYRLTLVKAW NVDELQAYAQ LVSLGNPDFI 

       610        620        630        640        650        660 
EVKGVTYCGE SSASSLTMAH VPWHEEVVQF VHELVDLIPE YEIACEHEHS NCLLIAHRKF 

       670        680        690        700        710        720 
KIGGEWWTWI DYNRFQELIQ EYEDSGGSKT FSAKDYMART PHWALFGASE RGFDPKDTRH 

       730 
QRKNKSKAIS GC 

« Hide

Isoform 2 [UniParc].

Checksum: 43A06B3E5DFC86C6
Show »

FASTA38443,700

References

[1]"Complete sequencing and characterization of 21,243 full-length human cDNAs."
Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S. expand/collapse author list , Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K., Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A., Sudo H., Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M., Takahashi M., Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y., Abe K., Kamihara K., Katsuta N., Sato K., Tanikawa M., Yamazaki M., Ninomiya K., Ishibashi T., Yamashita H., Murakawa K., Fujimori K., Tanai H., Kimata M., Watanabe M., Hiraoka S., Chiba Y., Ishida S., Ono Y., Takiguchi S., Watanabe S., Yosida M., Hotuta T., Kusano J., Kanehori K., Takahashi-Fujii A., Hara H., Tanase T.-O., Nomura Y., Togiya S., Komai F., Hara R., Takeuchi K., Arita M., Imose N., Musashino K., Yuuki H., Oshima A., Sasaki N., Aotsuka S., Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S., Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O., Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H., Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B., Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y., Fujimori Y., Komiyama M., Tashiro H., Tanigami A., Fujiwara T., Ono T., Yamada K., Fujii Y., Ozaki K., Hirao M., Ohmori Y., Kawabata A., Hikiji T., Kobatake N., Inagaki H., Ikema Y., Okamoto S., Okitani R., Kawakami T., Noguchi S., Itoh T., Shigeta K., Senba T., Matsumura K., Nakajima Y., Mizuno T., Morinaga M., Sasaki M., Togashi T., Oyama M., Hata H., Watanabe M., Komatsu T., Mizushima-Sugano J., Satoh T., Shirai Y., Takahashi Y., Nakagawa K., Okumura K., Nagase T., Nomura N., Kikuchi H., Masuho Y., Yamashita R., Nakai K., Yada T., Nakamura Y., Ohara O., Isogai T., Sugano S.
Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1), VARIANTS ARG-632 AND ASN-671.
Tissue: Teratocarcinoma.
[2]"The DNA sequence of human chromosome 7."
Hillier L.W., Fulton R.S., Fulton L.A., Graves T.A., Pepin K.H., Wagner-McPherson C., Layman D., Maas J., Jaeger S., Walker R., Wylie K., Sekhon M., Becker M.C., O'Laughlin M.D., Schaller M.E., Fewell G.A., Delehaunty K.D., Miner T.L. expand/collapse author list , Nash W.E., Cordes M., Du H., Sun H., Edwards J., Bradshaw-Cordum H., Ali J., Andrews S., Isak A., Vanbrunt A., Nguyen C., Du F., Lamar B., Courtney L., Kalicki J., Ozersky P., Bielicki L., Scott K., Holmes A., Harkins R., Harris A., Strong C.M., Hou S., Tomlinson C., Dauphin-Kohlberg S., Kozlowicz-Reilly A., Leonard S., Rohlfing T., Rock S.M., Tin-Wollam A.-M., Abbott A., Minx P., Maupin R., Strowmatt C., Latreille P., Miller N., Johnson D., Murray J., Woessner J.P., Wendl M.C., Yang S.-P., Schultz B.R., Wallis J.W., Spieth J., Bieri T.A., Nelson J.O., Berkowicz N., Wohldmann P.E., Cook L.L., Hickenbotham M.T., Eldred J., Williams D., Bedell J.A., Mardis E.R., Clifton S.W., Chissoe S.L., Marra M.A., Raymond C., Haugen E., Gillett W., Zhou Y., James R., Phelps K., Iadanoto S., Bubb K., Simms E., Levy R., Clendenning J., Kaul R., Kent W.J., Furey T.S., Baertsch R.A., Brent M.R., Keibler E., Flicek P., Bork P., Suyama M., Bailey J.A., Portnoy M.E., Torrents D., Chinwalla A.T., Gish W.R., Eddy S.R., McPherson J.D., Olson M.V., Eichler E.E., Green E.D., Waterston R.H., Wilson R.K.
Nature 424:157-164(2003) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[3]"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 1 AND 2).
Tissue: Colon, Placenta and Uterus.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AK001762 mRNA. Translation: BAA91891.1.
AK022917 mRNA. Translation: BAB14307.1. Different initiation.
AC079920 Genomic DNA. No translation available.
AC006480 Genomic DNA. Translation: AAS07568.1.
AC073089 Genomic DNA. Translation: AAS07520.1.
BC015591 mRNA. Translation: AAH15591.1. Frameshift.
BC042156 mRNA. Translation: AAH42156.1. Different termination.
BC051888 mRNA. Translation: AAH51888.1.
IPIIPI00182304.
IPI00844116.
RefSeqNP_060734.2. NM_018264.3.
UniGeneHs.520917.

3D structure databases

HSSPHSSP built from PDB template 1TLL based on UniProtKB P29476.
ProteinModelPortalQ9NV66.
ModBaseSearch...

Protein-protein interaction databases

IntActQ9NV66. 1 interaction.
STRING9606.ENSP00000352645.

PTM databases

PhosphoSiteQ9NV66.

Polymorphism databases

DMDM143678193.

Proteomic databases

PaxDbQ9NV66.
PRIDEQ9NV66.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000359626; ENSP00000352645; ENSG00000198874.
ENST00000361660; ENSP00000354795; ENSG00000198874.
GeneID55253.
KEGGhsa:55253.
UCSCuc003tvn.3. human.

Organism-specific databases

CTD55253.
GeneCardsGC07P066460.
H-InvDBHIX0006729.
HGNCHGNC:25598. TYW1.
HPAHPA015535.
MIM611243. gene.
neXtProtNX_Q9NV66.
PharmGKBPA134940167.
GenAtlasSearch...

Phylogenomic databases

eggNOGCOG0731.
HOVERGENHBG108623.
InParanoidQ9NV66.
KOK15449.
OMAERREMIT.
OrthoDBEOG4548Z4.
PhylomeDBQ9NV66.

Enzyme and pathway databases

UniPathwayUPA00375.

Gene expression databases

ArrayExpressQ9NV66.
BgeeQ9NV66.
CleanExHS_TYW1.
GenevestigatorQ9NV66.

Family and domain databases

Gene3D3.20.20.70. 1 hit.
InterProIPR013785. Aldolase_TIM.
IPR001094. Flavdoxin.
IPR008254. Flavodoxin/NO_synth.
IPR007197. rSAM.
IPR013917. tRNA_wybutosine-synth.
[Graphical view]
PfamPF00258. Flavodoxin_1. 1 hit.
PF04055. Radical_SAM. 1 hit.
PF08608. Wyosine_form. 1 hit.
[Graphical view]
PRINTSPR00369. FLAVODOXIN.
PROSITEPS50902. FLAVODOXIN_LIKE. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

GenomeRNAi55253.
NextBio59324.
SOURCESearch...

Entry information

Entry nameTYW1_HUMAN
AccessionPrimary (citable) accession number: Q9NV66
Secondary accession number(s): Q6PJG8 expand/collapse secondary AC list , Q75MG8, Q75MN3, Q86V12, Q8IVS7, Q9H9C4
Entry history
Integrated into UniProtKB/Swiss-Prot: April 3, 2007
Last sequence update: April 3, 2007
Last modified: May 1, 2013
This is version 85 of the entry and version 2 of the sequence. [Complete history]
Entry statusReviewed (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.

Relevant documents

Human chromosome 7

Human chromosome 7: entries, gene names and cross-references to MIM

Human entries with polymorphisms or disease mutations

List of human entries with polymorphisms or disease mutations

Human polymorphisms and disease mutations

Index of human polymorphisms and disease mutations

MIM cross-references

Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot

PATHWAY comments

Index of metabolic and biosynthesis pathways

SIMILARITY comments

Index of protein domains and families