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_RS05040 BPHYT_RS05040 sugar ABC transporter ATPase

Query= BRENDA::Q70HW1
         (384 letters)



>FitnessBrowser__BFirm:BPHYT_RS05040
          Length = 371

 Score =  352 bits (903), Expect = e-101
 Identities = 183/377 (48%), Positives = 251/377 (66%), Gaps = 15/377 (3%)

Query: 1   MARVLLEHIYKTYPGQTEPTVKDFNLDIQDKEFTVFVGPSGCGKTTTLRMIAGLEDITEG 60
           MA + +  +YKTYP    P +K  N+DI+D +F + VG SGCGK+T L MIAGLE +T+G
Sbjct: 1   MASLSIRDVYKTYPNGV-PVLKGVNIDIEDGQFLILVGGSGCGKSTLLNMIAGLETVTKG 59

Query: 61  NLYIGDRRVNDVPPKDRDIAMVFQNYALYPHMTVYQNMAFGLKLRKVPKAEIDRRVQEAA 120
            + I  + VN++ PKDRDIAMVFQ+YALYP MTV +N++FGL +RKVPK E  + V   +
Sbjct: 60  EIQIDGKTVNNLSPKDRDIAMVFQSYALYPSMTVRENISFGLNIRKVPKNEQTQIVDRVS 119

Query: 121 KILDIAHLLDRKPKALSGGQRQRVALGRAIVREPQVFLMDEPLSNLDAKLRVQMRAEIRK 180
             L I HLLDRKP  LSGGQRQRVA+GRA+ R+P +FL DEPLSNLDAKLR++MR+EI+ 
Sbjct: 120 NTLQITHLLDRKPGQLSGGQRQRVAMGRALARDPVMFLFDEPLSNLDAKLRIEMRSEIKL 179

Query: 181 LHQRLQTTVIYVTHDQTEAMTMGDRIVVMRDGVIQQADTPQVVYSQPKNMFVAGFIGSPA 240
           LHQRL TT++YVTHDQ EAMT+GDRI VM+DG++QQ   PQ +Y  P N+FVAGFIG+P 
Sbjct: 180 LHQRLGTTIVYVTHDQIEAMTLGDRIAVMKDGIVQQFGAPQEIYDSPSNLFVAGFIGAPP 239

Query: 241 MNFIRGEIVQDGDAFYFRAPS----ISLRLPEGRYGVLKASGAIGKPVVLGVRPEDLHDE 296
           MNFI+G++V+ G        +     +L LP   +   K    +G+ V+LG+RPE + D 
Sbjct: 240 MNFIQGKLVEQGAGVALELDTGVARTALNLP---FDSAKVRSHVGREVILGLRPERITDA 296

Query: 297 EVFMTTYPDSV----LQMQVEVVEHMGSEVYLHTSIGPNTIVARVNPRHVYHVGSSVKLA 352
                 + D+     ++++V+V+E  G +  +   +    IV+RV+P       ++  L 
Sbjct: 297 R---GAHGDNAKLQPIEVKVDVIEPTGPDTLVFAQVNGKRIVSRVHPASNPQPLANTTLL 353

Query: 353 IDLNKIHIFDAETEESI 369
            D +K  +FD   EE I
Sbjct: 354 FDTSKAVLFDPSNEERI 370


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: 393
Number of extensions: 15
Number of successful extensions: 4
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: 371
Length adjustment: 30
Effective length of query: 354
Effective length of database: 341
Effective search space:   120714
Effective search space used:   120714
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