Alignments for a candidate for H281DRAFT_01113 in Rhizobium leguminosarum 3841

GapMind for catabolism of small carbon sources

Alignments for a candidate for H281DRAFT_01113 in Rhizobium leguminosarum 3841

Align deoxynucleoside transporter, ATPase component (characterized)
to candidate WP_011653997.1 RL_RS23960 sugar ABC transporter ATP-binding protein

Query= reanno::Burk376:H281DRAFT_01113
         (515 letters)



>NCBI__GCF_000009265.1:WP_011653997.1
          Length = 513

 Score =  338 bits (867), Expect = 3e-97
 Identities = 177/496 (35%), Positives = 304/496 (61%), Gaps = 7/496 (1%)

Query: 8   SAPLSQPFLEVVGVHKRFTGVHALRGVSLSFQRGQIYHLLGENGCGKSTLIKIISGAQPP 67
           + P ++  L   GV K F GV AL  V    +R  ++ L+GENG GKSTL+KI++G   P
Sbjct: 16  AVPNAEYLLSAEGVRKEFPGVVALDDVQFRLKRASVHALMGENGAGKSTLMKILAGIYTP 75

Query: 68  DEGQLVIEGVPHARLSALEALAAGIETVYQDLSLLPNMSVAENVALTSELATHEGRLART 127
           D+G + ++G+     S L+AL  GI  ++Q+L+L+P M+VAEN+ +  E     G +   
Sbjct: 76  DKGDIRLKGIEIQLKSPLDALENGIAMIHQELNLMPFMTVAENIWIRREPKNRLGFI--- 132

Query: 128 FDRRVLAATAARALEAVGLPGNSEFQSTLIEQLPLATRQLVAIARAIASEAKFVIMDEPT 187
            D  V+          + +  + + +   +  L +A RQ+V IA+A++  +  +IMDEPT
Sbjct: 133 -DHGVMHRMTEELFTRLNIAIDPDIE---VRFLSVANRQMVEIAKAVSYNSDVLIMDEPT 188

Query: 188 TSLTQKEVDNLIAVLANLRAQGVTVLFVSHKLDECYAIGGEVIVLRDGQKMAQGPIAEFT 247
           ++LT++EV++L  ++ +L+AQG+ +++++HK++E + I  E  V RDG+ +      + T
Sbjct: 189 SALTEREVEHLFRIIRDLKAQGIGIVYITHKMNELFEIADEFSVFRDGRYIGTHASTDVT 248

Query: 248 KAQISELMTGRHLSNERYRESAHAQDIVLDVRGFTRAGQFSDVSFKLHGGEILGVTGLLD 307
           +  I  +M GR ++    +E     +++L V+     G F +VSF++  GEILGV GL+ 
Sbjct: 249 RDDIIRMMVGREITQMFPKEEVPIGEVMLSVKDLCLNGVFKNVSFEVRAGEILGVAGLVG 308

Query: 308 SGRNELARALAGVAPAQSGDVLLDGQQIALRTPSDAKRHRIGYVPEDRLNEGLFLDKPIR 367
           SGR+ +A  L GV PA SG + L G+ +A+ +P++A R+R+ ++ EDR + G  L   I 
Sbjct: 309 SGRSNVAETLFGVTPASSGSIELYGKPVAISSPTEAIRNRMAFLTEDRKDTGCLLILDIL 368

Query: 368 DNVITAMISSLRDRFGQIDRTRAQALAEQTVKELQIATPGVDKPVQSLSGGNQQRVLIGR 427
           +N+  A++     + G + +   +A  E   K+L++ TP + + V++LSGGNQQ+VLIGR
Sbjct: 369 ENMQIAVLQDRYVKGGFVQQGAVEATCEDMAKKLRVKTPNLYERVENLSGGNQQKVLIGR 428

Query: 428 WLAIDPRVLILHGPTVGVDVGSKDIIYRIMQRLSQRGIGIILISDDLPELLQNCDRILMM 487
           WL  +PR+LIL  PT G+DVG+K  I+R++  +++ G+ +++IS ++PE+L   DRI++M
Sbjct: 429 WLLTNPRILILDEPTRGIDVGAKAEIHRLVTEMARDGVAVVMISSEMPEVLGMSDRIMVM 488

Query: 488 KKGHVSAEYRADELSE 503
            +G V+     DE ++
Sbjct: 489 HEGRVTGFLNRDEATQ 504



 Score = 79.3 bits (194), Expect = 3e-19
 Identities = 58/223 (26%), Positives = 110/223 (49%), Gaps = 6/223 (2%)

Query: 289 DVSFKLHGGEILGVTGLLDSGRNELARALAGVAPAQSGDVLLDGQQIALRTPSDAKRHRI 348
           DV F+L    +  + G   +G++ L + LAG+     GD+ L G +I L++P DA  + I
Sbjct: 41  DVQFRLKRASVHALMGENGAGKSTLMKILAGIYTPDKGDIRLKGIEIQLKSPLDALENGI 100

Query: 349 GYVPEDRLNEGLFLDKPIRDNVITAMISSLRDRFGQIDRTRAQALAEQTVKELQIATPGV 408
             + ++ LN   F+   + +N+        ++R G ID      + E+    L IA    
Sbjct: 101 AMIHQE-LNLMPFMT--VAENIWIRR--EPKNRLGFIDHGVMHRMTEELFTRLNIAIDP- 154

Query: 409 DKPVQSLSGGNQQRVLIGRWLAIDPRVLILHGPTVGVDVGSKDIIYRIMQRLSQRGIGII 468
           D  V+ LS  N+Q V I + ++ +  VLI+  PT  +     + ++RI++ L  +GIGI+
Sbjct: 155 DIEVRFLSVANRQMVEIAKAVSYNSDVLIMDEPTSALTEREVEHLFRIIRDLKAQGIGIV 214

Query: 469 LISDDLPELLQNCDRILMMKKGHVSAEYRADELSEADLYHALL 511
            I+  + EL +  D   + + G     + + +++  D+   ++
Sbjct: 215 YITHKMNELFEIADEFSVFRDGRYIGTHASTDVTRDDIIRMMV 257


Lambda     K      H
   0.319    0.135    0.376 

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: 588
Number of extensions: 34
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: 515
Length of database: 513
Length adjustment: 35
Effective length of query: 480
Effective length of database: 478
Effective search space:   229440
Effective search space used:   229440
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 (21.7 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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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