GapMind for catabolism of small carbon sources

 

Alignments for a candidate for citA in Cupriavidus basilensis 4G11

Align Citrate:H+ symporter (characterized)
to candidate RR42_RS19610 RR42_RS19610 MFS transporter

Query= TCDB::P16482
         (444 letters)



>FitnessBrowser__Cup4G11:RR42_RS19610
          Length = 432

 Score =  310 bits (793), Expect = 8e-89
 Identities = 171/418 (40%), Positives = 238/418 (56%), Gaps = 5/418 (1%)

Query: 29  AILRVTSGNFLEQFDFFLFGFYATYIAHTFFPASSEFASLMMTFAVFGAGFLMRPIGAIV 88
           AIL  T GN LE FDF ++ F+A  IA  FFP  ++  S ++T A FG GF MRP+GAIV
Sbjct: 15  AILAATIGNGLEWFDFTVYSFFALIIAKLFFPTGNDLTSFLLTVATFGVGFFMRPVGAIV 74

Query: 89  LGAYIDKVGRRKGLIVTLSIMATGTFLIVLIPSYQTIGLWAPLLVLIGRLLQGFSAGAEL 148
           LG Y D+VGR+  L +T+ +MA GT +I L P+Y +IGLWAP L+++ RL+QGFSAG E+
Sbjct: 75  LGVYADRVGRKAALTLTILMMALGTAIIGLAPTYSSIGLWAPALIVLARLIQGFSAGGEV 134

Query: 149 GGVSVYLAEIATPGRKGFYTSWQSGSQQVAIMVAAAMGFALNAVLEPSAISDWGWRIPFL 208
           GG + +L E A    +G Y SWQ  SQ ++ M+ AAMG  +   LEP  I  WGWRIPFL
Sbjct: 135 GGATAFLIEHAPDEERGAYASWQQASQGISFMLGAAMGALVINGLEPEQIDAWGWRIPFL 194

Query: 209 FGVLIVPFIFILRRKLEETQEFTARRHHLAMRQV-----FATLLANWQVVIAGMMMVAMT 263
           FG+LI P    +R  LEE   F ARR   A  +V        L  + + V+AG+ +  + 
Sbjct: 195 FGLLIGPVGMYIRSHLEEPPAFEARRAERAASKVKFSPLTQVLRDHPREVLAGLGVTILW 254

Query: 264 TTAFYLITVYAPTFGKKVLMLSASDSLLVTLLVAISNFFWLPVGGALSDRFGRRSVLIAM 323
           T   Y++  Y P++ K+ L L    +   T L         P+ G LSDR GR+ +L  +
Sbjct: 255 TVCTYVLVFYMPSYAKQQLGLPLGATFQSTALCGAIILVLCPLMGMLSDRVGRKRMLGTV 314

Query: 324 TLLALATAWPALTMLANAPSFLMMLSVLLWLSFIYGMYNGAMIPALTEIMPAEVRVAGFS 383
            L+    A+P    L  +P+   +L V + L  +   + G     L E  P EVR  G S
Sbjct: 315 ALIIGVLAYPLFHWLNVSPTTQTLLMVQVILGILLAAFTGPAPAVLAEQFPTEVRSTGLS 374

Query: 384 LAYSLATAVFGGFTPVISTALIEYTGDKASPGYWMSFAAICGLLATCYLYRRSAVALQ 441
           LAY+ A  +FGGF P+I T LI  +G K +P Y++  AA    +A  +++ R+   LQ
Sbjct: 375 LAYNFAVTIFGGFAPLIVTWLIASSGSKLAPAYYVIAAAAISFVALLFMHDRTGKPLQ 432


Lambda     K      H
   0.329    0.139    0.421 

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: 529
Number of extensions: 25
Number of successful extensions: 2
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: 444
Length of database: 432
Length adjustment: 32
Effective length of query: 412
Effective length of database: 400
Effective search space:   164800
Effective search space used:   164800
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.9 bits)
S2: 51 (24.3 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:

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