Alignments for a candidate for HSERO_RS03640 in Klebsiella variicola At-22

GapMind for catabolism of small carbon sources

Alignments for a candidate for HSERO_RS03640 in Klebsiella variicola At-22

Align Ribose import ATP-binding protein RbsA; EC 7.5.2.7 (characterized, see rationale)
to candidate WP_012969141.1 KVAR_RS23745 sugar ABC transporter ATP-binding protein

Query= uniprot:D8IZC7
         (521 letters)



>NCBI__GCF_000025465.1:WP_012969141.1
          Length = 506

 Score =  540 bits (1392), Expect = e-158
 Identities = 284/502 (56%), Positives = 371/502 (73%), Gaps = 6/502 (1%)

Query: 1   MTQTPLLQMRGIRKSFGATLALSDMHLTIRPGEIHALMGENGAGKSTLMKVLSGVHAPDQ 60
           MT TP+L+MR I K+FG   AL  + LT+ PGEIHALMGENGAGKSTLMK+L+G +    
Sbjct: 1   MTATPVLEMRHIAKAFGKFYALKGVDLTVWPGEIHALMGENGAGKSTLMKILAGAYTATS 60

Query: 61  GEILLDGRPVALRDPGASRAAGINLIYQELAVAPNISVAANVFMGSELRTRLGLIDHAAM 120
           GEIL+DG+P  +R P  + AAGI LIYQE+ +APN++VA N+F+GSEL  R GL+   AM
Sbjct: 61  GEILIDGKPQTIRGPKDALAAGITLIYQEMQLAPNLTVAENIFLGSEL-ARGGLVQRKAM 119

Query: 121 RSRTDAVLRQLGAGFGASDLAGRLSIAEQQQVEIARALVHRSRIVIMDEPTAALSERETE 180
            S+  AV+ +LGA F ASD    L+IAEQQQVEIARAL  +SRI++MDEPTAALS RET+
Sbjct: 120 LSQAQAVIDRLGAQFKASDRVMTLTIAEQQQVEIARALHRQSRILVMDEPTAALSSRETQ 179

Query: 181 QLFNVVRRLRDEGLAIIYISHRMAEVYALADRVTVLRDGSFVGELVRDEIDSERIVQMMV 240
           +LF ++ RLRDEG+AIIYISHRMAEVY L+DRV+VLRDG +VG LVRD++++  +V+MMV
Sbjct: 180 RLFELILRLRDEGMAIIYISHRMAEVYELSDRVSVLRDGQYVGSLVRDKLNAPELVRMMV 239

Query: 241 GRSLSEFYQHQRIAPADAAQLPTVMQVRALA-GGKIRPASFDVRAGEVLGFAGLVGAGRT 299
           GR LS+ +  +R  P    +L    +V  L  GGK++P+S  V AGE++G AGLVGAGR+
Sbjct: 240 GRPLSDLFNKERDIPRGQPRL----RVEDLTDGGKVKPSSLVVHAGEIVGLAGLVGAGRS 295

Query: 300 ELARLLFGADPRSGGDILLEGRPVHIDQPRAAMRAGIAYVPEDRKGQGLFLQMAVAANAT 359
           ELA+L+FG    +GG I ++G PV I  PR A+  GI ++ E+RK QGLFL++A   N T
Sbjct: 296 ELAQLIFGVRKATGGVIEIDGEPVVIHSPREAIDLGIGFLTENRKEQGLFLELAAQENIT 355

Query: 360 MNVASRHTRLGLVRSRSLGGVARAAIQRLNVKVAHPETPVGKLSGGNQQKVLLARWLEIA 419
           M    R    G++  R    ++  AIQ LN++V H +   G LSGGNQQK+L++RW+ I 
Sbjct: 356 MATLERDANWGMLNRRKAQTISDDAIQLLNIRVPHAQVRAGGLSGGNQQKLLISRWVAIG 415

Query: 420 PKVLILDEPTRGVDIYAKSEIYQLVHRLASQGVAVVVISSELPEVIGICDRVLVMREGMI 479
           P++LILDEPTRGVD+ AKSEIY++++ +A QGVA+++ISSELPEV+G+ DRV VMREG I
Sbjct: 416 PRILILDEPTRGVDVGAKSEIYRIMNDMARQGVAILMISSELPEVVGMSDRVYVMREGAI 475

Query: 480 TGELAGAAITQENIMRLATDTN 501
            GEL    I+QENIM LAT  N
Sbjct: 476 AGELQAGDISQENIMTLATGVN 497


Lambda     K      H
   0.320    0.135    0.378 

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: 773
Number of extensions: 34
Number of successful extensions: 7
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: 521
Length of database: 506
Length adjustment: 35
Effective length of query: 486
Effective length of database: 471
Effective search space:   228906
Effective search space used:   228906
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 (21.8 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.

Downloads

Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

Related tools

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