Protein WP_110207765.1 in Nocardioides daejeonensis MJ31
Annotation: NCBI__GCF_003194585.1:WP_110207765.1
Length: 412 amino acids
Source: GCF_003194585.1 in NCBI
Candidate for 25 steps in catabolism of small carbon sources
Pathway | Step | Score | Similar to | Id. | Cov. | Bits | Other hit | Other id. | Other bits |
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) | 48% | 95% | 355.5 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
L-proline catabolism | proV | med | glycine betaine/l-proline transport atp-binding protein prov (characterized) | 45% | 99% | 328.6 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
L-histidine catabolism | hutV | med | ABC transporter for L-Histidine, ATPase component (characterized) | 55% | 96% | 287 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
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) | 54% | 96% | 285 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
L-asparagine catabolism | aatP | med | ABC transporter for L-aspartate, L-asparagine, L-glutamate, and L-glutamine, ATPase component (characterized) | 40% | 94% | 157.5 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
L-aspartate catabolism | aatP | med | ABC transporter for L-aspartate, L-asparagine, L-glutamate, and L-glutamine, ATPase component (characterized) | 40% | 94% | 157.5 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
L-glutamate catabolism | gltL | med | ABC transporter for L-aspartate, L-asparagine, L-glutamate, and L-glutamine, ATPase component (characterized) | 40% | 94% | 157.5 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
L-histidine catabolism | PA5503 | lo | Methionine import ATP-binding protein MetN 2, component of L-Histidine uptake porter, MetIQN (characterized) | 38% | 74% | 171.8 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
putrescine catabolism | potA | lo | spermidine/putrescine ABC transporter, ATP-binding protein PotA; EC 3.6.3.31 (characterized) | 33% | 83% | 170.2 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
L-arabinose catabolism | xacJ | lo | Xylose/arabinose import ATP-binding protein XacJ; EC 7.5.2.13 (characterized, see rationale) | 38% | 58% | 161.8 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
N-acetyl-D-glucosamine catabolism | SMc02869 | lo | N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) | 37% | 68% | 159.1 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
D-glucosamine (chitosamine) catabolism | SMc02869 | lo | N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) | 37% | 68% | 159.1 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
L-arabinose catabolism | xacK | lo | Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale) | 39% | 58% | 157.5 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
L-asparagine catabolism | glnQ | lo | Glutamine ABC transporter ATP-binding protein, component of Glutamine transporter, GlnQP. Takes up glutamine, asparagine and glutamate which compete for each other for binding both substrate and the transmembrane protein constituent of the system (Fulyani et al. 2015). Tandem substrate binding domains (SBDs) differ in substrate specificity and affinity, allowing cells to efficiently accumulate different amino acids via a single ABC transporter. Analysis revealed the roles of individual residues in determining the substrate affinity (characterized) | 36% | 98% | 152.9 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
D-maltose catabolism | malK_Bb | lo | ABC-type maltose transport, ATP binding protein (characterized, see rationale) | 34% | 67% | 152.1 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
D-sorbitol (glucitol) catabolism | mtlK | lo | ABC transporter for D-Sorbitol, ATPase component (characterized) | 32% | 76% | 149.8 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
trehalose catabolism | treV | lo | TreV, component of Trehalose porter (characterized) | 33% | 65% | 141 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
D-maltose catabolism | aglK | lo | ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized) | 34% | 65% | 139.4 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
D-maltose catabolism | thuK | lo | ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized) | 34% | 65% | 139.4 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
sucrose catabolism | aglK | lo | ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized) | 34% | 65% | 139.4 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
trehalose catabolism | aglK | lo | ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized) | 34% | 65% | 139.4 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
L-histidine catabolism | hisP | lo | histidine transport ATP-binding protein hisP (characterized) | 36% | 89% | 138.7 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
L-asparagine catabolism | peb1C | lo | PEB1C, component of Uptake system for glutamate and aspartate (characterized) | 36% | 91% | 136.7 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
L-aspartate catabolism | peb1C | lo | PEB1C, component of Uptake system for glutamate and aspartate (characterized) | 36% | 91% | 136.7 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
L-citrulline catabolism | AO353_03040 | lo | ABC transporter for L-Arginine and L-Citrulline, ATPase component (characterized) | 31% | 98% | 136.7 | Glycine betaine/carnitine transport ATP-binding protein GbuA; EC 7.6.2.9 | 48% | 360.5 |
Sequence Analysis Tools
View WP_110207765.1 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
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Sequence
MSLIELSGVHKIFGKRPQRALARLQSGATREELRADGITAAVIDASFTVDPGQIFVVMGL
SGSGKSTLIRMVNGLLEPTSGSVVVAGEDLARLDARKLRRARREKVSMVFQHFALLPHRT
VGENAAYALKVKGMNRSDRQRQAEQALEMVGLGGWGGSLPGDLSGGMRQRVGLARALAAG
TEVMLMDEAFSALDPLIRREMQDQLIELQNQLGKTILFITHDLNEAMRLGDRIAMMRDGR
IVQQGTAEQILNDPANDYVAQFVQDVDRTKVLTAASIMERPVAVLGAGQGPRAAHKLMRE
NQLNALMVVDRQHNLRGLITEATAAEAVKTGQESLDGLVTPAHQVTPDTCVADLFTAAAE
RPEPLAVVEGTKLAGVIARVTLLSALGNLNGSETAAGELVSAGSATTDGGQA
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