Q53T40 (Q53T40_HUMAN) Unreviewed, UniProtKB/TrEMBL

Names and origin

Protein names

Submitted name:
Putative uncharacterized protein FHL2 EMBL AAY15012.1

Gene names

Name:

FHL2 EMBL AAY15012.1

Organism

Homo sapiens (Human) EMBL AAY15012.1

Taxonomic identifier

9606 [NCBI]

Taxonomic lineage

cellular organisms › Eukaryota › Opisthokonta › Metazoa › Eumetazoa › Bilateria › Deuterostomia › Chordata › Craniata › Vertebrata › Gnathostomata › Teleostomi › Euteleostomi › Sarcopterygii › Tetrapoda › Amniota › Mammalia › Theria › Eutheria › Euarchontoglires › Primates › Haplorrhini › Simiiformes › Catarrhini › Hominoidea › Hominidae › Homininae › Homo

Protein attributes

Sequence length	168 AA.
Sequence status	Fragment.
Protein existence	Evidence at transcript level

General annotation (Comments)

Sequence similarities

Contains 3 LIM zinc-binding domains. RuleBase RU000350

Ontologies

Keywords
Domain	LIM domain RuleBase RU000350 SAAS SAAS001781
Ligand	Metal-binding Zinc
Gene Ontology (GO)
Biological_process	atrial cardiac muscle cell development Inferred from electronic annotation. Source: Compara heart trabecula formation Inferred from electronic annotation. Source: Compara negative regulation of transcription, DNA-dependent Inferred from electronic annotation. Source: Compara osteoblast differentiation Inferred from electronic annotation. Source: Compara regulation of transcription from RNA polymerase II promoter Inferred from electronic annotation. Source: Compara ventricular cardiac muscle cell development Inferred from electronic annotation. Source: Compara
Cellular_component	M band Inferred from electronic annotation. Source: Compara Z disc Inferred from electronic annotation. Source: Compara nucleus Inferred from electronic annotation. Source: Compara
Molecular_function	zinc ion binding Inferred from electronic annotation. Source: InterPro
Complete GO annotation...

Sequence annotation (Features)

	Feature key	Position(s)	Length	Description	Graphical view	Feature identifier
Experimental info
	Non-terminal residue	1	1	EMBL AAY15012.1

Sequences

	Sequence		Length	Mass (Da)
	Q53T40 [UniParc]. Last modified May 24, 2005. Version 1. Checksum: FA61C05DC1999ACF	FASTA	168	19,307
	10 20 30 40 50 60 TRKMEYKGSS WHETCFICHR CQQPIGTKSF IPKDNQNFCV PCYEKQHAMQ CVQCKKPITT 70 80 90 100 110 120 GGVTYREQPW HKECFVCTAC RKQLSGQRFT ARDDFAYCLN CFCDLYAKKC AGCTNPISGL 130 140 150 160 GGTKYISFEE RQWHNDCFNC KKCSLSLVGR GFLTERDDIL CPDCGKDI

References

[1]	"The sequence of Homo sapiens BAC clone RP11-332H14." Haakenson W., Mulvaney E. Submitted (OCT-1999) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE.
[2]	Waterston R.H. Submitted (AUG-2001) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE.
[3]	Waterston R. Submitted (JAN-2002) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE.
[4]	Wilson R.K. Submitted (APR-2005) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE.

Cross-references

Sequence databases
EMBL GenBank DDBJ	AC012360 Genomic DNA. Translation: AAY15012.1.
IPI	IPI00743342.
UniGene	Hs.443687.
3D structure databases
ModBase	Search...
Protein-protein interaction databases
STRING	Q53T40.
Proteomic databases
PRIDE	Q53T40.
Protocols and materials databases
StructuralBiologyKnowledgebase	Search...
Phylogenomic databases
HOVERGEN	HBG074526.
Gene expression databases
ArrayExpress	Q53T40.
Bgee	Q53T40.
Family and domain databases
Gene3D	2.10.110.10. 3 hits.
InterPro	IPR001781. Znf_LIM. [Graphical view]
Pfam	PF00412. LIM. 3 hits. [Graphical view]
SMART	SM00132. LIM. 3 hits. [Graphical view]
PROSITE	PS00478. LIM_DOMAIN_1. 2 hits. PS50023. LIM_DOMAIN_2. 3 hits. [Graphical view]
ProtoNet	Search...
Other
ChiTaRS	FHL2. human.

Entry information

Entry name

Q53T40_HUMAN

Accession

Primary (citable) accession number: Q53T40

Entry history

Integrated into UniProtKB/TrEMBL:	May 24, 2005
Last sequence update:	May 24, 2005
Last modified:	April 3, 2013
This is version 42 of the entry and version 1 of the sequence. [Complete history]

Entry status

Unreviewed (UniProtKB/TrEMBL)

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.