GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Aa in Sinorhizobium meliloti 1021

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate SM_b21106 SM_b21106 sugar ABC transporter ATP-binding protein

Query= BRENDA::Q70HW1
         (384 letters)



>FitnessBrowser__Smeli:SM_b21106
          Length = 365

 Score =  338 bits (868), Expect = 1e-97
 Identities = 188/373 (50%), Positives = 254/373 (68%), Gaps = 14/373 (3%)

Query: 1   MARVLLEHIYKTYPGQTEPTVKDFNLDIQDKEFTVFVGPSGCGKTTTLRMIAGLEDITEG 60
           MA V L+ + K Y G  E  V   +L+++D+EF   VGPSGCGK+TTLRMIAGLE+++ G
Sbjct: 1   MAPVTLKKLVKRY-GALE-VVHGIDLEVKDREFIALVGPSGCGKSTTLRMIAGLEEVSGG 58

Query: 61  NLYIGDRRVNDVPPKDRDIAMVFQNYALYPHMTVYQNMAFGLKLRKVPKAEIDRRVQEAA 120
            + IG R+VND+PP+ R+I+MVFQ+YALYPHMTV +NM F LK+   P  EI  RV EAA
Sbjct: 59  AIEIGGRKVNDLPPRARNISMVFQSYALYPHMTVAENMGFSLKIAGRPAEEIKTRVAEAA 118

Query: 121 KILDIAHLLDRKPKALSGGQRQRVALGRAIVREPQVFLMDEPLSNLDAKLRVQMRAEIRK 180
            ILD+AHLL+R+P  LSGGQRQRVA+GRAIVR+P VFL DEPLSNLDAKLR Q+R EI+K
Sbjct: 119 AILDLAHLLERRPSQLSGGQRQRVAMGRAIVRQPDVFLFDEPLSNLDAKLRTQVRTEIKK 178

Query: 181 LHQRLQTTVIYVTHDQTEAMTMGDRIVVMRDGVIQQADTPQVVYSQPKNMFVAGFIGSPA 240
           LH R+Q T+IYVTHDQ EAMT+ DRIV+MRDG I+Q  TP+ V+ +P   FVAGFIGSP 
Sbjct: 179 LHARMQATMIYVTHDQVEAMTLSDRIVIMRDGHIEQVGTPEDVFRRPATKFVAGFIGSPP 238

Query: 241 MNFIRGEIVQDGDAFYFRAPSISLRLPEGRYGVLKASGAIGKPVVLGVRPEDLHDE-EVF 299
           MN +   ++ DG   +  A   +L LP     +++     G+ V  G+RP+D++      
Sbjct: 239 MN-MEEAVLTDGKLAF--ASGATLPLPPRFRSLVRE----GQKVTFGLRPDDVYPSGHGL 291

Query: 300 MTTYPDSV--LQMQVEVVEHMGSEVYLHTSIGPNTIVAR-VNPRHVYHVGSSVKLAIDLN 356
                D+V  +++ V + E +G+E  + T       V+R +NPR +   G +V ++ DL 
Sbjct: 292 HAGDADAVHEIELPVTITEPLGNETLVFTQFNGRDWVSRMLNPRPL-RPGEAVPMSFDLA 350

Query: 357 KIHIFDAETEESI 369
           + H+FD ET  ++
Sbjct: 351 RAHLFDGETGRAL 363


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: 415
Number of extensions: 17
Number of successful extensions: 2
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: 365
Length adjustment: 30
Effective length of query: 354
Effective length of database: 335
Effective search space:   118590
Effective search space used:   118590
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: 50 (23.9 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