GapMind for catabolism of small carbon sources

 

Alignments for a candidate for citA in Klebsiella michiganensis M5al

Align Citrate:H+ symporter (characterized)
to candidate BWI76_RS21415 BWI76_RS21415 MFS transporter

Query= TCDB::P16482
         (444 letters)



>FitnessBrowser__Koxy:BWI76_RS21415
          Length = 432

 Score =  235 bits (599), Expect = 2e-66
 Identities = 136/387 (35%), Positives = 207/387 (53%), Gaps = 18/387 (4%)

Query: 26  RIGAILRVTSGNFLEQFDFFLFGFYATYIAHTFFPASSEFASLMMTFAVFGAGFLMRPIG 85
           RI AI+  +SGN +E FDF+++ F + Y AH FFP+ +    L+ T  VF AGFLMRPIG
Sbjct: 20  RIWAIVGASSGNLVEWFDFYVYSFCSLYFAHIFFPSGNTTTQLLQTAGVFAAGFLMRPIG 79

Query: 86  AIVLGAYIDKVGRRKGLIVTLSIMATGTFLIVLIPSYQTIGLWAPLLVLIGRLLQGFSAG 145
             + G   D+ GR+  +++++ +M  G+ +I  +P Y TIG WAP L+L+ RL QG S G
Sbjct: 80  GWIFGRIADRRGRKTSMLISVCMMCFGSLVIACLPGYATIGTWAPALLLLARLFQGLSVG 139

Query: 146 AELGGVSVYLAEIATPGRKGFYTSWQ----SGSQQVAIMVAAAMGFALNAVLEPSAISDW 201
            E G  + Y++E+A  G+KGFY S+Q     G Q +A++V      AL  +L   A+  W
Sbjct: 140 GEYGTSATYMSEVAVEGKKGFYASFQYVTLIGGQLLAVLVVV----ALQQILSDEALHAW 195

Query: 202 GWRIPFLFGVLIVPFIFILRRKLEETQEFTARRHHLAMRQVFATLLANWQVVIAGMMMVA 261
           GWRIPF  G ++      LRR+L+ET +   R   L     F  L  N +  I  +   A
Sbjct: 196 GWRIPFALGAVLAIVALWLRRQLDETSKQETRA--LKEAGSFKGLWRNRKAFIMVLGFTA 253

Query: 262 MTTTAFYLITVYAPTFGKKVLMLSASDSLLVTLLVAISNFFWLPVGGALSDRFGRRSVLI 321
             + +FY  T Y   +      ++A  + ++            P+ GALSD+ GRR+ ++
Sbjct: 254 AGSLSFYTFTTYMQKYLVNTAGMTAGTASMIMTAALFVYMLVQPLFGALSDKIGRRTSML 313

Query: 322 AMTLLALATAWPALTMLANAPS----FLMMLSVLLWLSFIYGMYNGAMIPALTEIMPAEV 377
              +L      P L  L N  S    F +++  LL +SF Y   +G +     E+ PA+V
Sbjct: 314 CFGVLVTVFTVPILNALQNVSSPYAAFALVICALLIVSF-YTSISGIL---KAEMFPAQV 369

Query: 378 RVAGFSLAYSLATAVFGGFTPVISTAL 404
           R  G  L+Y++A A+FGG    ++ +L
Sbjct: 370 RALGVGLSYAVANALFGGSAEYVALSL 396


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: 511
Number of extensions: 27
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: 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