GapMind for catabolism of small carbon sources

 

Aligments for a candidate for gltL in Bacteroides thetaiotaomicron VPI-5482

Align PP1068, component of Acidic amino acid uptake porter, AatJMQP (characterized)
to candidate 350849 BT1321 putative phosphate transport ATP-binding protein (NCBI ptt file)

Query= TCDB::Q88NY5
         (256 letters)



>lcl|FitnessBrowser__Btheta:350849 BT1321 putative phosphate
           transport ATP-binding protein (NCBI ptt file)
          Length = 252

 Score =  136 bits (343), Expect = 4e-37
 Identities = 92/247 (37%), Positives = 132/247 (53%), Gaps = 16/247 (6%)

Query: 10  DLRMISIKNVNKWYGDFQVLTDCSTEVKKGEVVVVCGPSGSGKSTLIKCVNALEPF---- 65
           D   I  ++VN WYGDF  L   S ++++  VV   GPSG GKST ++  N +       
Sbjct: 2   DTVKIDTRDVNFWYGDFHALKGISMQIEEKSVVAFIGPSGCGKSTFLRLFNRMNDLIPAT 61

Query: 66  -QKGDIVVDGTSIADPKTNLPKLRSRVGMVFQHFELFPHLTITENLTIAQR------KVL 118
             +G+I +DG +I      + +LR  VGMVFQ    FP  +I EN+    R         
Sbjct: 62  RLEGEIRIDGHNIYAKGVEVDELRKNVGMVFQRPNPFPK-SIFENVAYGLRVNGVKDNAF 120

Query: 119 GRSEAEATKKGLALLDRVGLSAHAKKHPGQLSGGQQQRVAIARALAMDPIVMLFDEPTSA 178
            R   E T KG AL D V      K+    LSGGQQQR+ IARA+A+ P V+L DEP SA
Sbjct: 121 IRQRVEETLKGAALWDEV--KDKLKESAYALSGGQQQRLCIARAMAVSPSVLLMDEPASA 178

Query: 179 LDPEMVSEVLDVMVQLAQEGMTMMCVTHEMGFARKVANRVIFMDKGSIIE-DCTKEEFFG 237
           LDP   ++V +++ +L ++  T++ VTH M  A +V+++  F   G ++E D TK+ F  
Sbjct: 179 LDPISTAKVEELIHELKKD-YTIVIVTHNMQQAARVSDKTAFFYLGEMVEYDDTKKIFTN 237

Query: 238 DQSARDQ 244
            +    Q
Sbjct: 238 PEKEATQ 244


Lambda     K      H
   0.319    0.134    0.383 

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: 112
Number of extensions: 4
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: 256
Length of database: 252
Length adjustment: 24
Effective length of query: 232
Effective length of database: 228
Effective search space:    52896
Effective search space used:    52896
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: 47 (22.7 bits)

This GapMind analysis is from Sep 17 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:

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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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