Alignments for a candidate for PS417_11890 in Phyllobacterium brassicacearum STM 196

GapMind for catabolism of small carbon sources

Alignments for a candidate for PS417_11890 in Phyllobacterium brassicacearum STM 196

Align Inositol transport system ATP-binding protein (characterized)
to candidate WP_106709787.1 CU102_RS04475 sugar ABC transporter ATP-binding protein

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



>NCBI__GCF_003010955.1:WP_106709787.1
          Length = 514

 Score =  410 bits (1053), Expect = e-119
 Identities = 226/501 (45%), Positives = 326/501 (65%), Gaps = 8/501 (1%)

Query: 18  LEEPYLLEIVNISKGFPGVVALADVQLRVRPGTVLALMGENGAGKSTLMKIIAGIYQPDA 77
           + EP +L I N++K F  V AL +V   +  G V AL GENGAGKSTLM IIAG+ QPD 
Sbjct: 1   MREP-VLSIRNVTKHFGAVKALTNVNFALERGEVHALCGENGAGKSTLMNIIAGVLQPDE 59

Query: 78  GEIRLRGKPIVFETPLAAQKAGIAMIHQELNLMPHMSIAENIWIGREQLNSLHMVNHREM 137
           GEI L GK +   +P AAQ  G+ ++HQE+ L P  S+AENI++         ++N+R++
Sbjct: 60  GEIVLDGKTVRIGSPAAAQSLGLGLVHQEIALCPDASVAENIFMASISRQRSLLMNYRKL 119

Query: 138 HRCTAELLARLRINLDPEEQVGNLSIAERQMVEIAKAVSYDSDILIMDEPTSAITEKEVA 197
            R    +++RL   +D   +VG L I+ +Q+VEIAKA++ D  +LI DEPT+A+TE E  
Sbjct: 120 EREAQAVMSRLA-PIDVRRKVGELPISSQQLVEIAKALTLDCRVLIFDEPTAALTEAEAR 178

Query: 198 HLFSIIADLKSQGKGIVYITHKMNEVFAIADEVAVFRDGHYIGLQRADSMNSDSLISMMV 257
            LF II DLK+ G  IVYI+H+M E+F + D V V RDG Y+   R   +  D ++  MV
Sbjct: 179 ILFEIIRDLKANGISIVYISHRMAEIFELCDRVTVLRDGRYVSTDRVADLTPDDVVRRMV 238

Query: 258 GRELSQLFPLRETPIGD----LLLTVRDLTLDGVFKDVSFDLHAGEILGIAGLMGSGRTN 313
           GRE++QL+P ++ P G+    ++ +VR L  +  F+DV  DL  GEILGI GL+GSGRT 
Sbjct: 239 GREITQLYPPKQ-PAGERPQEVVFSVRGLGDNERFRDVDIDLTRGEILGIGGLIGSGRTE 297

Query: 314 VAETIFGITPSSSGQITLDGKAVRISDPHMAIEKGFALLTEDRKLSGLFPCLSVLENMEM 373
           +AE I G+  +++GQI + GK   I     A++ G   L+EDRK SGLF  LS+ +N+ +
Sbjct: 298 IAEGICGLRATTNGQILIHGKQQAIGTYADAVKAGLVYLSEDRKGSGLFLDLSIAKNISV 357

Query: 374 AVLPHYTGN-GFIQQKALRALCEDMCKKLRVKTPSLEQCIDTLSGGNQQKALLARWLMTN 432
             L   TG+ G I       L  D  ++L ++  S+   + +LSGGNQQK  +A+ L   
Sbjct: 358 LNLDALTGHLGLIDTVGEGDLARDFAQRLNIRMGSIGAPVSSLSGGNQQKVAIAKQLAIQ 417

Query: 433 PRLLILDEPTRGIDVGAKAEIYRLIAFLASEGMAVIMISSELPEVLGMSDRVMVMHEGEL 492
           P+++++DEPTRGIDVGAK+EI+ L+  LA  G+ +I+ISSELPE+LG+ DRV+V+ EGE+
Sbjct: 418 PKVILMDEPTRGIDVGAKSEIHALLRELAQSGIGIIVISSELPELLGLCDRVIVIREGEV 477

Query: 493 MGTLDRSEATQEKVMQLASGM 513
            G L   + T+E+V++LASG+
Sbjct: 478 AGELGMDDMTEERVIRLASGV 498


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: 605
Number of extensions: 26
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: 517
Length of database: 514
Length adjustment: 35
Effective length of query: 482
Effective length of database: 479
Effective search space:   230878
Effective search space used:   230878
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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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