GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_17605 in Roseburia faecis M72

Align ATP-binding cassette domain-containing protein; SubName: Full=Amino acid transporter; SubName: Full=Histidine ABC transporter ATP-binding protein; SubName: Full=Histidine transport system ATP-binding protein (characterized, see rationale)
to candidate WP_022046731.1 M72_RS03885 ABC transporter ATP-binding protein

Query= uniprot:A0A1N7U8S3
         (276 letters)



>NCBI__GCF_001406815.1:WP_022046731.1
          Length = 352

 Score =  125 bits (314), Expect = 1e-33
 Identities = 79/247 (31%), Positives = 135/247 (54%), Gaps = 18/247 (7%)

Query: 27  LQVEGIHKRYGEHEVLKGVSLNARQGDVISLIGASGSGKSTMLRCINFLEQPDAGVITLD 86
           +++  I K YG       VS    +G +++L+G SGSGK+T+LR I  LE P++G I +D
Sbjct: 3   VEMRDICKNYGNFRASDHVSFGIEKGKLVALLGPSGSGKTTLLRMIAGLETPNSGDIYID 62

Query: 87  GISIEMRQGRAGTRAPHQDQLQNLRTRLAMVFQHFNLWSHMTVLENITMAPRRVLDVSAA 146
           G  +              + +   +  +  VFQ++ L+ +MTV +N+      +  V   
Sbjct: 63  GQRV--------------NDVPAAKRGIGFVFQNYALFRYMTVYDNVAFG-LELAKVPKK 107

Query: 147 EAEKRARMYLDKVGLPSRVADQYPAFLSGGQQQRVAIARALAMEPEIILFDEPTSALDPE 206
           E +KR    L+  GL S +  +YP  LSGGQ+QRVA ARALA  P+++L DEP +A+D +
Sbjct: 108 EIKKRVTELLELTGL-SGMEKRYPNQLSGGQRQRVAFARALAPNPQVLLLDEPFAAIDAK 166

Query: 207 LVGEVLKVIQTLAEE-GRTMLMVTHEMGFARQVSSQVLFLHQGRVEEHG-DARILDQPNS 264
           +  E+   ++ +  + G T + VTH+   A +V+ +++  + G +E+ G    I   P++
Sbjct: 167 VRTELRNWLREMVVKLGITSIFVTHDQDEAVEVADEIIITNHGHIEQMGTPMEIYKSPDT 226

Query: 265 ERLQQFL 271
             + QF+
Sbjct: 227 PFVAQFI 233


Lambda     K      H
   0.319    0.133    0.372 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 218
Number of extensions: 10
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 276
Length of database: 352
Length adjustment: 27
Effective length of query: 249
Effective length of database: 325
Effective search space:    80925
Effective search space used:    80925
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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:

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:

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:

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