Protein WP_092348019.1 in Desulfuromusa kysingii DSM 7343
Annotation: NCBI__GCF_900107645.1:WP_092348019.1
Length: 417 amino acids
Source: GCF_900107645.1 in NCBI
Candidate for 12 steps in catabolism of small carbon sources
Pathway | Step | Score | Similar to | Id. | Cov. | Bits | Other hit | Other id. | Other bits |
L-proline catabolism | proV | hi | glycine betaine/l-proline transport atp-binding protein prov (characterized) | 59% | 99% | 446.8 | OtaA, component of The salt-induced glycine betaine OtaABC transporter | 50% | 396.7 |
L-proline catabolism | opuBA | med | BusAA, component of Uptake system for glycine-betaine (high affinity) and proline (low affinity) (OpuAA-OpuABC) or BusAA-ABC of Lactococcus lactis). BusAA, the ATPase subunit, has a C-terminal tandem cystathionine β-synthase (CBS) domain which is the cytoplasmic K+ sensor for osmotic stress (osmotic strength)while the BusABC subunit has the membrane and receptor domains fused to each other (Biemans-Oldehinkel et al., 2006; Mahmood et al., 2006; Gul et al. 2012). An N-terminal amphipathic α-helix of OpuA is necessary for high activity but is not critical for biogenesis or the ionic regulation of transport (characterized) | 47% | 99% | 364.8 | glycine betaine/l-proline transport atp-binding protein prov | 59% | 446.8 |
L-histidine catabolism | hutV | med | ABC transporter for L-Histidine, ATPase component (characterized) | 58% | 95% | 304.3 | glycine betaine/l-proline transport atp-binding protein prov | 59% | 446.8 |
L-proline catabolism | hutV | med | HutV aka HISV aka R02702 aka SMC00670, component of Uptake system for hisitidine, proline, proline-betaine and glycine-betaine (characterized) | 57% | 95% | 300.8 | glycine betaine/l-proline transport atp-binding protein prov | 59% | 446.8 |
L-arginine catabolism | artP | lo | ABC transporter for L-Arginine, putative ATPase component (characterized) | 36% | 95% | 152.5 | glycine betaine/l-proline transport atp-binding protein prov | 59% | 446.8 |
L-histidine catabolism | Ac3H11_2560 | lo | ABC transporter for L-Histidine, ATPase component (characterized) | 38% | 80% | 152.5 | glycine betaine/l-proline transport atp-binding protein prov | 59% | 446.8 |
L-lysine catabolism | hisP | lo | ABC transporter for L-Lysine, ATPase component (characterized) | 36% | 96% | 150.6 | glycine betaine/l-proline transport atp-binding protein prov | 59% | 446.8 |
L-histidine catabolism | hisP | lo | Histidine transport ATP-binding protein HisP (characterized) | 35% | 91% | 150.2 | glycine betaine/l-proline transport atp-binding protein prov | 59% | 446.8 |
L-asparagine catabolism | bztD | lo | BztD, component of Glutamate/glutamine/aspartate/asparagine porter (characterized) | 34% | 85% | 149.4 | glycine betaine/l-proline transport atp-binding protein prov | 59% | 446.8 |
L-aspartate catabolism | bztD | lo | BztD, component of Glutamate/glutamine/aspartate/asparagine porter (characterized) | 34% | 85% | 149.4 | glycine betaine/l-proline transport atp-binding protein prov | 59% | 446.8 |
L-citrulline catabolism | AO353_03040 | lo | ABC transporter for L-Arginine and L-Citrulline, ATPase component (characterized) | 33% | 98% | 145.2 | glycine betaine/l-proline transport atp-binding protein prov | 59% | 446.8 |
L-tryptophan catabolism | ecfA1 | lo | Energy-coupling factor transporter ATP-binding protein EcfA1; Short=ECF transporter A component EcfA; EC 7.-.-.- (characterized, see rationale) | 37% | 81% | 142.5 | glycine betaine/l-proline transport atp-binding protein prov | 59% | 446.8 |
Sequence Analysis Tools
View WP_092348019.1 at NCBI
Find papers: PaperBLAST
Find functional residues: SitesBLAST
Search for conserved domains
Find the best match in UniProt
Compare to protein structures
Predict transmenbrane helices: Phobius
Predict protein localization: PSORTb
Find homologs in fast.genomics
Fitness BLAST: loading...
Sequence
MEEEVKLEVRNLYKIFGPFPKKAMAMLEQGLDKEEIFEKTETTVGVQNASFRIYEGEIFV
IMGLSGSGKSTMVRMFNRLIEPTAGQVLIDGEDITVMNSDQLVKLRRAKLSMVFQSFALM
PHMTVLQNAAFGLEMDGIDKSTRQKRALEALEQVGLEAWAESMPNELSGGMQQRVGLARG
LAVDPDILLMDEAFSALDPLIRTEMQDELLKLQSKSKRTIVFISHDLDEAMRIGDRIAIM
EGGRVVQVGTPEEILQNPADDYVRAFFRGVDPTNILSAGDIATATQVTIPITDGKNPRTG
LQRLIKNDRDYAFVLDRDKVFKGIVSTDSLHAMLESDDIPHLIPNAYLEGVVAAHKDDSL
QDILPHVAGHSWPLPILDDEGRFIGAVSKNLFLRTLHRSSDEEQLPEEPQGNGAIAS
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.
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About GapMind
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using
ublast (a fast alternative to protein BLAST)
against a database of manually-curated proteins (most of which are experimentally characterized) or by using
HMMer with enzyme models (usually from
TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
- ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
- HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.
where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").
Otherwise, a candidate is "medium confidence" if either:
- ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
- ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
- HMMer finds a hit (regardless of coverage or other bits).
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps."
For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways.
For diverse bacteria and archaea that can utilize a carbon source, there is a complete
high-confidence catabolic pathway (including a transporter) just 38% of the time, and
there is a complete medium-confidence pathway 63% of the time.
Gaps may be due to:
- our ignorance of proteins' functions,
- omissions in the gene models,
- frame-shift errors in the genome sequence, or
- the organism lacks the pathway.
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory