GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK in Pseudovibrio axinellae Ad2

Align MalK, component of Maltose/Maltotriose/maltodextrin (up to 7 glucose units) transporters MalXFGK (MsmK (3.A.1.1.28) can probably substitute for MalK; Webb et al., 2008) (characterized)
to candidate WP_068002943.1 PsAD2_RS04510 ABC transporter ATP-binding protein

Query= TCDB::Q8DT25
         (377 letters)



>NCBI__GCF_001623255.1:WP_068002943.1
          Length = 363

 Score =  331 bits (848), Expect = 2e-95
 Identities = 177/379 (46%), Positives = 250/379 (65%), Gaps = 20/379 (5%)

Query: 1   MTTLKLDNIYKRYPNAKHYSVENFNLDIHDKEFIVFVGPSGCGKSTTLRMIAGLEDITEG 60
           M  ++L+N+ KRY + +   +   NL++ + EF VFVGPSGCGK+TTLRMIAGLE +++G
Sbjct: 1   MPRIRLENLVKRYGDFE--VLHGINLEMEENEFTVFVGPSGCGKTTTLRMIAGLETVSDG 58

Query: 61  NLYIDDKLMNDASPKDRDIAMVFQNYALYPHMSVYENMAFGLKLRKYKKDDINKRVHEAA 120
            +YI D+ ++   PK RD+AMVFQ+YALYPHM+V +NM+F L+L++  + +I+++V   A
Sbjct: 59  EIYIGDRPVSQLEPKARDLAMVFQDYALYPHMNVAKNMSFALRLQRRPRKEIDEKVGLVA 118

Query: 121 EILGLTEFLERKPADLSGGQRQRVAMGRAIVRDAKVFLMDEPLSNLDAKLRVAMRAEIAK 180
           E+LGLT+FL RKP +LSGGQRQRVAMGRA+ RDA  FL DEPLSNLDAKLR  MRAE+A 
Sbjct: 119 EMLGLTKFLHRKPGELSGGQRQRVAMGRALARDAGTFLFDEPLSNLDAKLRCQMRAELAI 178

Query: 181 IHRRIGATTIYVTHDQTEAMTLADRIVIMSATPNPDKTGSIGRIEQIGTPQELYNEPANK 240
           + +++    IYVTHDQ EAMTL DRIV+M+           G I+Q GTP+EL+ +PANK
Sbjct: 179 MRQKVRKNMIYVTHDQIEAMTLGDRIVVMNG----------GYIQQQGTPEELFKQPANK 228

Query: 241 FVAGFIGSPAMNFFEVTVEK---ERLVNQDGLSLALPQGQEKILEEKGYLGKKVTLGIRP 297
           FVAGF+GSP MNF    ++    +  V+ DG  +ALP  +E+     G+    V LGIRP
Sbjct: 229 FVAGFLGSPPMNFLGAKIQDLGGQVFVSGDGFEVALP--EERASVALGHSASSVILGIRP 286

Query: 298 EDISSDQIVHETFPNASVTADILVSELLGSESMLYVKFGSTEFTARVNARDSHSPGEKVQ 357
            D+       +   + ++   ++VSE +G++S+L    G+ +    + +    + GE ++
Sbjct: 287 SDLHFSPHAPD---HEAIDLKVIVSEYIGAQSVLLCNCGAQKIEVELKSETPIALGETLR 343

Query: 358 LTFNIAKGHFFDLETEKRI 376
              N    H FD ETE  I
Sbjct: 344 FAVNREAIHLFDSETEVAI 362


Lambda     K      H
   0.318    0.135    0.379 

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: 360
Number of extensions: 11
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: 377
Length of database: 363
Length adjustment: 30
Effective length of query: 347
Effective length of database: 333
Effective search space:   115551
Effective search space used:   115551
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 49 (23.5 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:

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