GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PGA1_c12660 in Marinobacter adhaerens HP15

Align D-lactate transporter, permease component 2 (characterized)
to candidate GFF3113 HP15_3056 high-affinity branched-chain amino acid ABC transporter, permease protein

Query= reanno::Phaeo:GFF1250
         (340 letters)



>FitnessBrowser__Marino:GFF3113
          Length = 307

 Score =  132 bits (333), Expect = 9e-36
 Identities = 99/334 (29%), Positives = 161/334 (48%), Gaps = 42/334 (12%)

Query: 7   QILNGLDKGSAYALIALGLTLIFGTLGVVNFAHGALFMIGAFCAVTVQRVLSLSFETVDE 66
           Q++NGL  GS YALIA+G T+++G +G++NFAHG ++MIGA+ A+     L+        
Sbjct: 10  QLINGLTIGSTYALIAIGYTMVYGIIGMINFAHGEIYMIGAYTALIAITGLAA------- 62

Query: 67  TQKDFLGNPLKVKTPYVESWFGPEVGGAIIDWAVPLAILFAIPIMIGVGYVMERGLIKHF 126
                                   +G A +   + +A+L A+ +   +G+ +ER   +  
Sbjct: 63  ------------------------LGIAWLPLILIVALLCAMIVSSSMGWAVERVAYRPV 98

Query: 127 YKRPHADQILVTFGLAIVLQEVVKYFYGANPIQTPAPDALNGVVNLGSIIGMDIVYPVWR 186
             R     ++   G++I LQ  V    G+  I  PA   ++G  N GS  G  +     +
Sbjct: 99  RGRHRLIPLISAIGMSIFLQNYVHLAQGSRNIGFPA--LIDGGFNFGSGDGFQMSLSYMQ 156

Query: 187 VVYFFFAVVIIGGIFSFLQFTTFGMVVRAGMADRETVGLLGINIDRRFTIMFGIAAAVAG 246
           +  F   ++ +  +  F+  +  G   RA   D     LLGI+ +R  +  F I AA+A 
Sbjct: 157 ITIFITTLICMTALSLFISRSRTGRACRAVSQDLGMANLLGIDTNRIISATFVIGAALAA 216

Query: 247 LAGV---MYTPINSPNYHMGMDFLVLSFVVVVVGGMGSLPGAVLAGFLLGVLESFASMNE 303
           +AG+   MY     P +  G    + +F   V+GG+GS+PGA+L G +LGV ES  S   
Sbjct: 217 VAGLLLGMYYGSVDPLF--GFIAGLKAFTAAVLGGIGSIPGAMLGGLILGVAESMTS--- 271

Query: 304 IKSLIPGIDQIIIYVVAIIILLTRPRGLMGRKGV 337
              L      +I + + I+ILL +P GL+G+  V
Sbjct: 272 -GYLSGEYKDVISFSLLILILLFKPTGLLGKPEV 304


Lambda     K      H
   0.329    0.147    0.439 

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: 243
Number of extensions: 16
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: 340
Length of database: 307
Length adjustment: 28
Effective length of query: 312
Effective length of database: 279
Effective search space:    87048
Effective search space used:    87048
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 (21.8 bits)
S2: 48 (23.1 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