GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Aa in Burkholderia phytofirmans PsJN

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate BPHYT_RS35680 BPHYT_RS35680 sugar ABC transporter ATP-binding protein

Query= BRENDA::Q70HW1
         (384 letters)



>FitnessBrowser__BFirm:BPHYT_RS35680
          Length = 360

 Score =  345 bits (885), Expect = 1e-99
 Identities = 193/368 (52%), Positives = 244/368 (66%), Gaps = 16/368 (4%)

Query: 1   MARVLLEHIYKTYPGQTEPTVKDFNLDIQDKEFTVFVGPSGCGKTTTLRMIAGLEDITEG 60
           MA V L  I+K Y G T+  V   +LDI D EF V VGPSGCGK+T +RM+AGLE+I+ G
Sbjct: 1   MAAVQLSGIFKRY-GDTQ-VVHGIDLDIDDGEFVVLVGPSGCGKSTLMRMVAGLEEISGG 58

Query: 61  NLYIGDRRVNDVPPKDRDIAMVFQNYALYPHMTVYQNMAFGLKLRKVPKAEIDRRVQEAA 120
           +L IG  R N + P+ R+I+MVFQ+YALYPH++VY+N+AFG ++RK   A    R++ AA
Sbjct: 59  DLMIGGTRANSLAPQQRNISMVFQSYALYPHLSVYENIAFGPRIRKESSASFKPRIEAAA 118

Query: 121 KILDIAHLLDRKPKALSGGQRQRVALGRAIVREPQVFLMDEPLSNLDAKLRVQMRAEIRK 180
           K+L++   LDR P+ALSGGQRQRVA+GRA+VREP +FL DEPLSNLDAKLRVQMR EI+ 
Sbjct: 119 KMLNLGGYLDRLPRALSGGQRQRVAMGRAVVREPSLFLFDEPLSNLDAKLRVQMRTEIKA 178

Query: 181 LHQRLQTTVIYVTHDQTEAMTMGDRIVVMRDGVIQQADTPQVVYSQPKNMFVAGFIGSPA 240
           LHQRL+ TVIYVTHDQ EAMTM DRIVVM  G I+Q   P  +Y  P N+FVA F+GSP+
Sbjct: 179 LHQRLKNTVIYVTHDQIEAMTMADRIVVMNAGRIEQIGRPLELYDHPANLFVASFLGSPS 238

Query: 241 MNFIRGEIVQDGDAFYFRAPSISLRLPEGRYGVLK---ASGAIGKPVVLGVRPEDLHDEE 297
           MNF  G I     A   +   ++L L  G   VL+   AS  +G  V LGVRPE +    
Sbjct: 239 MNFAEGVI-----ASRAQGQGLALNLTGGGEIVLEGAPASAVVGAKVTLGVRPEHIET-- 291

Query: 298 VFMTTYPDSVLQMQVEVVEHMGSEVYLHTSIGPNTIVARVNPRHVYHVGSSVKLAIDLNK 357
             MT  PD+   M+VEVVE  G+E +L+  IG +T       R     G  V L +    
Sbjct: 292 --MTPTPDAT--MEVEVVEPTGAETHLYGKIGGSTWCVTTRQRSKIEPGQRVTLRLPAEH 347

Query: 358 IHIFDAET 365
           IH+FD E+
Sbjct: 348 IHLFDTES 355


Lambda     K      H
   0.321    0.138    0.395 

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: 404
Number of extensions: 13
Number of successful extensions: 3
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: 384
Length of database: 360
Length adjustment: 30
Effective length of query: 354
Effective length of database: 330
Effective search space:   116820
Effective search space used:   116820
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: 49 (23.5 bits)

This GapMind analysis is from Sep 17 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:

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:

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:

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:

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