GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gtsD in Rhodobacter viridis JA737

Align ABC transporter for D-Glucose-6-Phosphate, ATPase component (characterized)
to candidate WP_110804244.1 C8J30_RS03245 ABC transporter ATP-binding protein

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



>NCBI__GCF_003217355.1:WP_110804244.1
          Length = 332

 Score =  292 bits (747), Expect = 1e-83
 Identities = 162/362 (44%), Positives = 222/362 (61%), Gaps = 33/362 (9%)

Query: 1   MATLELRNVNKTYGAGLPDTLKNIELSIKEGEFLILVGPSGCGKSTLMNCIAGLETITGG 60
           M  + L+ V K +G    + +  I+L+I +GEF++ VGPSGCGKSTL+  IAGLE ++GG
Sbjct: 1   MGEIVLKGVTKRFGD--VEVIPPIDLAIHDGEFVVFVGPSGCGKSTLLRLIAGLEDVSGG 58

Query: 61  AIMIGDQDVSGMSPKDRDIAMVFQSYALYPTMSVRENIEFGLKIRKMPQADIDAEVARVA 120
            I I  +D +  +P DR +AMVFQSYALYP MSV++NI F LK+ K+P A+I+A+V   A
Sbjct: 59  KIEIDGKDATETAPSDRGLAMVFQSYALYPHMSVKKNIAFPLKMAKLPPAEIEAKVQAAA 118

Query: 121 KLLQIEHLLNRKPGQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEMKL 180
           K+L +   L+RKPGQLSGGQ+QRVA+GRA+ R P+ +LFDEPLSNLDA LRV MR E+  
Sbjct: 119 KVLNLSAYLDRKPGQLSGGQRQRVAIGRAIVRSPEAFLFDEPLSNLDAALRVNMRLEISE 178

Query: 181 MHQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPKEIYNNPANQFVASFIGSPP 240
           +H  LKTT +YVTHDQ+EAMT+ DK+ V++ G I+Q G+P E+Y  P N+FVA FIGSP 
Sbjct: 179 LHHTLKTTMIYVTHDQVEAMTMADKIVVLQAGRIEQVGSPLELYRTPRNRFVAGFIGSPK 238

Query: 241 MNFVPLRLQRKDGRLVALLDSGQARCELALNTTEAGLEDRDVILGLRPEQIMLAAGEGDS 300
           MNF+      K G                              +G+RPE I ++  EG  
Sbjct: 239 MNFIEGAEAAKHGAHA---------------------------IGIRPEHIRISTTEG-- 269

Query: 301 ASSIRAEVQVTEPTGPDTLVFVQLNDTKVCCRLAPDVAPQVGETLTLQFDPSKVLLFDAN 360
               +  V V+E  G DT + V      +  R   +V    G+++ L  D +++  FD  
Sbjct: 270 --MWKGTVGVSEHLGSDTFLHVTTEHGLLNVRAGGEVDLHHGDSVFLSPDMAQLHRFDKE 327

Query: 361 TG 362
            G
Sbjct: 328 GG 329


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: 325
Number of extensions: 8
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 386
Length of database: 332
Length adjustment: 29
Effective length of query: 357
Effective length of database: 303
Effective search space:   108171
Effective search space used:   108171
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