GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gtsD in Rhodobacter johrii JA192

Align ABC transporter for D-Galactose and D-Glucose, ATPase component (characterized)
to candidate WP_069332842.1 C8J29_RS18660 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= reanno::pseudo13_GW456_L13:PfGW456L13_1897
         (386 letters)



>NCBI__GCF_003046325.1:WP_069332842.1
          Length = 352

 Score =  352 bits (904), Expect = e-102
 Identities = 179/360 (49%), Positives = 247/360 (68%), Gaps = 12/360 (3%)

Query: 1   MATLELRNVNKTYGPGLPDTLKNIELKIDDGEFLILVGPSGCGKSTLMNCIAGLETISGG 60
           M+T+ +RNV K+Y       ++++   I DGEF++ VGPSGCGKSTL+  IAGLE+  GG
Sbjct: 1   MSTVHVRNVKKSYSD--LTVIEDLSFDIHDGEFMVFVGPSGCGKSTLLRMIAGLESFQGG 58

Query: 61  AILVDDADISGMSPKDRDIAMVFQSYALYPTMSVRDNIAFGLKIRKMPTAEIDEEVARVS 120
            + + +  ++G+  +DR+IAMVFQ YALYP M++RDN++FGLK+RK PTAEI+  VA  +
Sbjct: 59  EVAIGERVVNGVPARDRNIAMVFQDYALYPHMTIRDNMSFGLKMRKTPTAEIERRVAAAA 118

Query: 121 KLLQIEHLLSRKPGQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEMKL 180
           ++LQI HLL RKP  LSGGQ+QRVAMGRA+ R P ++LFDEPLSNLDAKLRVE+RTE+K 
Sbjct: 119 EILQIGHLLDRKPRALSGGQRQRVAMGRAIVREPDVFLFDEPLSNLDAKLRVEVRTEIKR 178

Query: 181 MHQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPKDIYNNPANLFVASFIGSPP 240
           +H RL  T +YVTHDQ+EAMT+ D++ V+K G ++Q GTP+++Y  P   FVA FIGSP 
Sbjct: 179 LHARLGATMIYVTHDQVEAMTMADRIVVLKGGAVEQIGTPQELYREPRTRFVAGFIGSPG 238

Query: 241 MNFIPLRLQRKDGRLLALLDSGQARCELPLGMQDAGLEDREVILGIRPEQIILANGEANG 300
           MNF P R++      +A L +G     +P+    +G    +  +GIRPE + LA+    G
Sbjct: 239 MNFAPARIEGD----VATLVTGD---RVPVRRLSSGTRAVQGEIGIRPEHVQLADPHGPG 291

Query: 301 LPTIRAEVQVTEPTGPDTLVFVNLNDTKVCCRLAPDVAPAVGETLTLQFDPAKVLLFDAK 360
           + T+   V V EP G DTLV V L + ++  RL  ++ PA G+ L L F P   + FDA+
Sbjct: 292 VETL---VDVVEPLGADTLVAVRLGEAQLMVRLPGEIIPAEGDRLRLSFTPGATMAFDAQ 348


Lambda     K      H
   0.319    0.138    0.393 

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: 412
Number of extensions: 15
Number of successful extensions: 4
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: 352
Length adjustment: 30
Effective length of query: 356
Effective length of database: 322
Effective search space:   114632
Effective search space used:   114632
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 (21.7 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