Alignments for a candidate for PS417_11890 in Rhizobium leguminosarum 3841

GapMind for catabolism of small carbon sources

Alignments for a candidate for PS417_11890 in Rhizobium leguminosarum 3841

Align Inositol transport system ATP-binding protein (characterized)
to candidate WP_011653997.1 RL_RS23960 sugar ABC transporter ATP-binding protein

Query= reanno::WCS417:GFF2332
         (517 letters)



>NCBI__GCF_000009265.1:WP_011653997.1
          Length = 513

 Score =  623 bits (1606), Expect = 0.0
 Identities = 318/491 (64%), Positives = 389/491 (79%), Gaps = 1/491 (0%)

Query: 22  YLLEIVNISKGFPGVVALADVQLRVRPGTVLALMGENGAGKSTLMKIIAGIYQPDAGEIR 81
           YLL    + K FPGVVAL DVQ R++  +V ALMGENGAGKSTLMKI+AGIY PD G+IR
Sbjct: 22  YLLSAEGVRKEFPGVVALDDVQFRLKRASVHALMGENGAGKSTLMKILAGIYTPDKGDIR 81

Query: 82  LRGKPIVFETPLAAQKAGIAMIHQELNLMPHMSIAENIWIGREQLNSLHMVNHREMHRCT 141
           L+G  I  ++PL A + GIAMIHQELNLMP M++AENIWI RE  N L  ++H  MHR T
Sbjct: 82  LKGIEIQLKSPLDALENGIAMIHQELNLMPFMTVAENIWIRREPKNRLGFIDHGVMHRMT 141

Query: 142 AELLARLRINLDPEEQVGNLSIAERQMVEIAKAVSYDSDILIMDEPTSAITEKEVAHLFS 201
            EL  RL I +DP+ +V  LS+A RQMVEIAKAVSY+SD+LIMDEPTSA+TE+EV HLF 
Sbjct: 142 EELFTRLNIAIDPDIEVRFLSVANRQMVEIAKAVSYNSDVLIMDEPTSALTEREVEHLFR 201

Query: 202 IIADLKSQGKGIVYITHKMNEVFAIADEVAVFRDGHYIGLQRADSMNSDSLISMMVGREL 261
           II DLK+QG GIVYITHKMNE+F IADE +VFRDG YIG   +  +  D +I MMVGRE+
Sbjct: 202 IIRDLKAQGIGIVYITHKMNELFEIADEFSVFRDGRYIGTHASTDVTRDDIIRMMVGREI 261

Query: 262 SQLFPLRETPIGDLLLTVRDLTLDGVFKDVSFDLHAGEILGIAGLMGSGRTNVAETIFGI 321
           +Q+FP  E PIG+++L+V+DL L+GVFK+VSF++ AGEILG+AGL+GSGR+NVAET+FG+
Sbjct: 262 TQMFPKEEVPIGEVMLSVKDLCLNGVFKNVSFEVRAGEILGVAGLVGSGRSNVAETLFGV 321

Query: 322 TPSSSGQITLDGKAVRISDPHMAIEKGFALLTEDRKLSGLFPCLSVLENMEMAVL-PHYT 380
           TP+SSG I L GK V IS P  AI    A LTEDRK +G    L +LENM++AVL   Y 
Sbjct: 322 TPASSGSIELYGKPVAISSPTEAIRNRMAFLTEDRKDTGCLLILDILENMQIAVLQDRYV 381

Query: 381 GNGFIQQKALRALCEDMCKKLRVKTPSLEQCIDTLSGGNQQKALLARWLMTNPRLLILDE 440
             GF+QQ A+ A CEDM KKLRVKTP+L + ++ LSGGNQQK L+ RWL+TNPR+LILDE
Sbjct: 382 KGGFVQQGAVEATCEDMAKKLRVKTPNLYERVENLSGGNQQKVLIGRWLLTNPRILILDE 441

Query: 441 PTRGIDVGAKAEIYRLIAFLASEGMAVIMISSELPEVLGMSDRVMVMHEGELMGTLDRSE 500
           PTRGIDVGAKAEI+RL+  +A +G+AV+MISSE+PEVLGMSDR+MVMHEG + G L+R E
Sbjct: 442 PTRGIDVGAKAEIHRLVTEMARDGVAVVMISSEMPEVLGMSDRIMVMHEGRVTGFLNRDE 501

Query: 501 ATQEKVMQLAS 511
           ATQ KVM+LA+
Sbjct: 502 ATQIKVMELAA 512



 Score = 90.5 bits (223), Expect = 1e-22
 Identities = 56/224 (25%), Positives = 115/224 (51%), Gaps = 7/224 (3%)

Query: 290 DVSFDLHAGEILGIAGLMGSGRTNVAETIFGITPSSSGQITLDGKAVRISDPHMAIEKGF 349
           DV F L    +  + G  G+G++ + + + GI     G I L G  +++  P  A+E G 
Sbjct: 41  DVQFRLKRASVHALMGENGAGKSTLMKILAGIYTPDKGDIRLKGIEIQLKSPLDALENGI 100

Query: 350 ALLTEDRKLSGLFPCLSVLENMEMAVLPHYTGNGFIQQKALRALCEDMCKKLRVKT-PSL 408
           A++ ++  L    P ++V EN+ +   P     GFI    +  + E++  +L +   P +
Sbjct: 101 AMIHQELNL---MPFMTVAENIWIRREPK-NRLGFIDHGVMHRMTEELFTRLNIAIDPDI 156

Query: 409 EQCIDTLSGGNQQKALLARWLMTNPRLLILDEPTRGIDVGAKAEIYRLIAFLASEGMAVI 468
           E  +  LS  N+Q   +A+ +  N  +LI+DEPT  +       ++R+I  L ++G+ ++
Sbjct: 157 E--VRFLSVANRQMVEIAKAVSYNSDVLIMDEPTSALTEREVEHLFRIIRDLKAQGIGIV 214

Query: 469 MISSELPEVLGMSDRVMVMHEGELMGTLDRSEATQEKVMQLASG 512
            I+ ++ E+  ++D   V  +G  +GT   ++ T++ ++++  G
Sbjct: 215 YITHKMNELFEIADEFSVFRDGRYIGTHASTDVTRDDIIRMMVG 258


Lambda     K      H
   0.320    0.136    0.381 

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: 680
Number of extensions: 26
Number of successful extensions: 6
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: 517
Length of database: 513
Length adjustment: 35
Effective length of query: 482
Effective length of database: 478
Effective search space:   230396
Effective search space used:   230396
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 Sep 24 2021. The underlying query database was built on Sep 17 2021.

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Protein sequences (fasta format)
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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 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