GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gtsD in Brucella inopinata BO1

Align ABC transporter for D-Glucose-6-Phosphate, ATPase component (characterized)
to candidate WP_008510203.1 BIBO1_RS16720 sn-glycerol-3-phosphate import ATP-binding protein UgpC

Query= reanno::WCS417:GFF4321
         (386 letters)



>NCBI__GCF_000182725.1:WP_008510203.1
          Length = 351

 Score =  302 bits (774), Expect = 8e-87
 Identities = 169/363 (46%), Positives = 231/363 (63%), Gaps = 21/363 (5%)

Query: 1   MATLELRNVNKTYGAGLPDTLKNIELSIKEGEFLILVGPSGCGKSTLMNCIAGLETITGG 60
           M+ + L NV K+YG  + + +K + L I +GEF++LVGPSGCGKSTL+  IAGLE+IT G
Sbjct: 1   MSKIVLDNVRKSYGGNI-EVIKGVSLEIADGEFVVLVGPSGCGKSTLLRMIAGLESITSG 59

Query: 61  AIMIGDQDVSGMSPKDRDIAMVFQSYALYPTMSVRENIEFGLKIRKMPQADIDAEVARVA 120
            I IG++ V+ + P +RDIAMVFQ+YALYP M+VREN+ +GLK RK P+ +I+  +A+ A
Sbjct: 60  TISIGERVVNNVEPAERDIAMVFQNYALYPHMTVRENLAYGLKNRKTPKEEIERRIAKAA 119

Query: 121 KLLQIEHLLNRKPGQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEMKL 180
           K L+IE  L RKP QLSGGQ+QRVAMGRA+ R P  +LFDEPLSNLDAKLRV+MR E+K 
Sbjct: 120 KALEIEQFLERKPRQLSGGQRQRVAMGRAIVREPAAFLFDEPLSNLDAKLRVQMRVEIKR 179

Query: 181 MHQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPKEIYNNPANQFVASFIGSPP 240
           + + L TT+VYVTHDQ+EAMT+ D++ V+  G I+Q GTP E+Y  PA+ FVA+FIGSP 
Sbjct: 180 LQRSLGTTSVYVTHDQMEAMTMADRLVVLNAGHIEQVGTPIELYEKPASTFVATFIGSPS 239

Query: 241 MNFVPLRLQRKDGRLVALLDSGQARCELALNTTEAGLEDRDVILGLRPEQIMLAAGEGDS 300
           MN     LQ  +    A    G A            L       G+RPE I +       
Sbjct: 240 MNL----LQSSES---AAWQPGSA----------ITLPSGGYTFGVRPEDIRILEEGDQD 282

Query: 301 ASSIRAEVQV--TEPTGPDTLVFVQLNDTK-VCCRLAPDVAPQVGETLTLQFDPSKVLLF 357
           A    A+V++   E  G ++ +   L+D K +  R+A      + E + +    + V +F
Sbjct: 283 ADGFNAQVRIEAVELVGAESYIHAALSDGKPLIFRVAGRSTHNIDEMVRVGASATDVHIF 342

Query: 358 DAN 360
            A+
Sbjct: 343 GAD 345


Lambda     K      H
   0.318    0.135    0.382 

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: 355
Number of extensions: 16
Number of successful extensions: 1
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: 386
Length of database: 351
Length adjustment: 30
Effective length of query: 356
Effective length of database: 321
Effective search space:   114276
Effective search space used:   114276
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 49 (23.5 bits)

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:

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