GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Sm in Stenotrophomonas chelatiphaga DSM 21508

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_057507764.1 ABB28_RS05960 polyamine ABC transporter ATP-binding protein

Query= TCDB::Q8DT25
         (377 letters)



>NCBI__GCF_001431535.1:WP_057507764.1
          Length = 378

 Score =  209 bits (533), Expect = 8e-59
 Identities = 127/323 (39%), Positives = 183/323 (56%), Gaps = 23/323 (7%)

Query: 20  SVENFNLDIHDKEFIVFVGPSGCGKSTTLRMIAGLEDITEGNLYIDDKLMNDASPKDRDI 79
           +V++ NLD+   E    +G SG GKST LR + G E  T G++ +D + +    P  R +
Sbjct: 35  AVDDVNLDVRKGEIFALLGGSGSGKSTLLRCLGGFETPTRGSIVLDGQPLVALPPYKRPV 94

Query: 80  AMVFQNYALYPHMSVYENMAFGLKLRKYKKDDINKRVHEAAEILGLTEFLERKPADLSGG 139
            M+FQ+YAL+PHMSV +N+AFGLK      D I +RV E  E++ +T   +R+P  LSGG
Sbjct: 95  NMMFQSYALFPHMSVEQNIAFGLKQDGLAGDAIRRRVGEMLELVHMTSLAKRRPHQLSGG 154

Query: 140 QRQRVAMGRAIVRDAKVFLMDEPLSNLDAKLRVAMRAEIAKIHRRIGATTIYVTHDQTEA 199
           Q+QRVA+ R++ +  K+ L+DEP+  LD KLR  M+ E+  I    G T + VTHDQ EA
Sbjct: 155 QQQRVALARSLAKGPKLLLLDEPMGALDKKLRSQMQLELVNIIETSGVTCVMVTHDQEEA 214

Query: 200 MTLADRIVIMSATPNPDKTGSIGRIEQIGTPQELYNEPANKFVAGFIGSPAMNFFEVTVE 259
           MT+A RI +M A          G I+Q+G P E+Y +PAN+FVAGFIGS  +N FE  ++
Sbjct: 215 MTMATRIAVMDA----------GWIQQVGKPDEVYEQPANRFVAGFIGS--VNSFEGVID 262

Query: 260 KERLVNQDGLSLALPQGQEKILEEKG---YLGKKVTLGIRPED--ISSDQIVHETFPNAS 314
           ++     + +++  P     I    G   Y G+ V   +RPE   I  D+    T     
Sbjct: 263 EDL---PEYVTVRSPAFPAPIYIGHGITCYEGQPVAFAVRPEKIIIGKDEPEGHTNKAQG 319

Query: 315 VTADILVSELLGSESMLYVKFGS 337
           V  DI      GS S+ +V+  S
Sbjct: 320 VIEDI---AYFGSHSVYHVRLPS 339


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: 334
Number of extensions: 14
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: 377
Length of database: 378
Length adjustment: 30
Effective length of query: 347
Effective length of database: 348
Effective search space:   120756
Effective search space used:   120756
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: 50 (23.9 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