GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Sm in Pseudomonas simiae WCS417

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 GFF2270 PS417_11575 spermidine/putrescine ABC transporter ATPase

Query= TCDB::Q8DT25
         (377 letters)



>FitnessBrowser__WCS417:GFF2270
          Length = 342

 Score =  219 bits (558), Expect = 9e-62
 Identities = 136/352 (38%), Positives = 199/352 (56%), Gaps = 36/352 (10%)

Query: 1   MTTLKLDNIYKRYPNAKHYSVENFNLDIHDKEFIVFVGPSGCGKSTTLRMIAGLEDITEG 60
           M  L+L+ + KRY      +V   +L +   EF+  +GPSGCGK+TTL+MIAG  D++ G
Sbjct: 1   MAFLQLNALSKRYGAVD--AVVATDLAVEKGEFVSLLGPSGCGKTTTLQMIAGFVDVSGG 58

Query: 61  NLYIDDKLMNDASPKDRDIAMVFQNYALYPHMSVYENMAFGLKLRKYKKDDINKRVHEAA 120
            + +D + +  A P  R + +VFQ+YAL+PHMSV +N+AFGLK+RK    +I  +V    
Sbjct: 59  QILLDGRDITHAKPASRGLGVVFQSYALFPHMSVRDNVAFGLKMRKVPAAEIASKVKTVL 118

Query: 121 EILGLTEFLERKPADLSGGQRQRVAMGRAIVRDAKVFLMDEPLSNLDAKLRVAMRAEIAK 180
           E++ L    +R P +LSGGQRQRVA+ RA+V +  V L+DEPLSNLDA LR  M+ EI +
Sbjct: 119 ELVRLAPHADRYPRELSGGQRQRVALARALVIEPPVLLLDEPLSNLDANLREEMQFEIRR 178

Query: 181 IHRRIGATTIYVTHDQTEAMTLADRIVIMSATPNPDKTGSIGRIEQIGTPQELYNEPANK 240
           I   +G TT+ VTHDQ EA++++DR+V+M A          GR+ QI  P +LY  P  +
Sbjct: 179 IQCAVGITTLMVTHDQAEALSISDRVVVMQA----------GRVTQIDAPYKLYEHPRTR 228

Query: 241 FVAGFIGSPAMNFFEVTVEKERLVNQDGLSLALPQGQEKILEEKGYLGKKVTLGIRPEDI 300
           F++ F+G            K  L+  D   L  PQ    +  E G    ++TL +RPE I
Sbjct: 229 FISDFVG------------KANLLPGDYDLLGSPQ----VRHESG--DGELTLSLRPEKI 270

Query: 301 SSDQIVHETFPNASVTADILVSELLGSESMLYVKFGSTEFTARVNARDSHSP 352
              Q+V     +  +   +L S   GS+ +  +     E T  V + D  +P
Sbjct: 271 ---QLVDA--GSGRLQGKVLDSYFFGSQWLYRIHTSLGEITV-VRSNDGSAP 316


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: 294
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: 342
Length adjustment: 29
Effective length of query: 348
Effective length of database: 313
Effective search space:   108924
Effective search space used:   108924
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 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