Alignments for a candidate for rbsA in Rhodobacter johrii JA192

GapMind for catabolism of small carbon sources

Alignments for a candidate for rbsA in Rhodobacter johrii JA192

Align Ribose import ATP-binding protein RbsA 2, component of D-ribose porter (Nanavati et al., 2006). Induced by ribose (characterized)
to candidate WP_069330308.1 C8J29_RS17445 sugar ABC transporter ATP-binding protein

Query= TCDB::Q9X051
         (523 letters)



>NCBI__GCF_003046325.1:WP_069330308.1
          Length = 497

 Score =  344 bits (883), Expect = 4e-99
 Identities = 195/502 (38%), Positives = 316/502 (62%), Gaps = 25/502 (4%)

Query: 10  EVLLEARNITKTFPGVIAVNNVTLQIYKGEVCALVGENGAGKSTLMKILAGVYPDYEGQI 69
           + L+E RNI K F GV A++ V+L I  GE+  L GENG+GKST++K+++G+Y   EG+I
Sbjct: 3   DTLIELRNIGKRFGGVRALDGVSLAIRPGEIHCLAGENGSGKSTVIKVMSGIYTPEEGEI 62

Query: 70  FLEGKEVRFRNPREAQENGIALIPQELDLVPNLSSAENIFLSREPVNEFGVIEYQKMFEQ 129
            ++G+ V   +P  A ++G+ +I Q+  L  NL+ AEN+ L+   +     +++++    
Sbjct: 63  LIDGRPVGRLDPIRAVQHGVQVIYQDFSLFGNLTVAENLALNTYVLEGRRRMDWRRARAM 122

Query: 130 ASKLFSKLGVNIDPKTKVEDLSTSQQQMVAIAKALSLDAKIIIMDEPTSAIGKRETEQLF 189
           A ++ +++GV+IDP  +V  L TS +Q+VAIA+A+   A++IIMDEPT+A+ + E + LF
Sbjct: 123 AVEVLARIGVDIDPDAEVGTLPTSGRQVVAIARAILARARLIIMDEPTTALTRHEVDALF 182

Query: 190 NIIRSLKNEGKSVIYISHRLEEIFEIADRVVVMRDGRKVGEGPIEEFDHDKLVRLMVGRS 249
            I+R L+ +G +V+++SH++ E+ EI++R+ V R+GRKV EGP+ +FD   +   M G S
Sbjct: 183 AIVRDLQAQGIAVLFVSHKMREMLEISERLTVFRNGRKVAEGPMSDFDEAAITHAMTGLS 242

Query: 250 IDQFFIKERATITDEIFR---VEGIKLWSLDRKKL----LVDDVSFYVRKGEVLGIYGLV 302
                      +TD+ +R     G  L  L+ +KL     V D+   +R GE++GI GL+
Sbjct: 243 -----------LTDDPYRPALPPGPPL--LEVRKLSVPGSVQDIDLSLRPGEIVGISGLI 289

Query: 303 GAGRTELLEAIFGAHPGRTEGKVFIGGKEIKIHSPRDAVKNGIGLVPEDRKTAGLILQMS 362
           G+GRTEL  A+FG  PG T G + +GG+EI   S ++A+  GI  VPEDR T GL L  S
Sbjct: 290 GSGRTELARALFGMEPGMT-GTIRLGGREIHPRSVQEAIALGIAYVPEDRLTEGLFLPQS 348

Query: 363 VLHNITLPSVVMKLIVRKFGLIDSQLEKEIVRSFIEKLNIKTPSPYQIVENLSGGNQQKV 422
           +  N+ + S++ +L  R+   +D++  +E        + I  PSP   V NLSGGN Q+V
Sbjct: 349 IERNLVV-SILERL--RRGPFLDTRAVREKTLGMFRDMQIAAPSPETAVGNLSGGNAQRV 405

Query: 423 VLAKWLAIKPKVLLLDEPTRGIDVNAKSEIYKLISEMAV-SGMGVVMVSSELPEILAMSD 481
           +L +WL    +VL+L+ PT G+DV +K+ I+++I ++A   G+GV+M+S ++PE++   +
Sbjct: 406 MLGRWLLTGARVLILNGPTVGVDVGSKATIHRIIRDLAQREGLGVLMISDDVPELVTNCN 465

Query: 482 RILVMSEGRKTAEFLREEVTEE 503
           RI VM  GR  A+     +TE+
Sbjct: 466 RIHVMHRGRFVADLDGSGMTED 487


Lambda     K      H
   0.317    0.137    0.372 

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: 542
Number of extensions: 25
Number of successful extensions: 8
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: 523
Length of database: 497
Length adjustment: 34
Effective length of query: 489
Effective length of database: 463
Effective search space:   226407
Effective search space used:   226407
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 (21.6 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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:

the paper from 2019 on GapMind for amino acid biosynthesis
the 2024 update on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources