GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuK in Pseudomonas putida KT2440

Align Trehalose/maltose import ATP-binding protein MalK; EC 7.5.2.1 (characterized)
to candidate PP_5137 PP_5137 ferric iron ABC transporter, ATP-binding protein

Query= SwissProt::Q9YGA6
         (372 letters)



>FitnessBrowser__Putida:PP_5137
          Length = 352

 Score =  237 bits (605), Expect = 3e-67
 Identities = 140/340 (41%), Positives = 205/340 (60%), Gaps = 14/340 (4%)

Query: 2   AGVRLVDVWKVFGEVTAVREMSLEVKDGEFMILLGPSGCGKTTTLRMIAGLEEPSRGQIY 61
           A +++ ++ K FG  TA+ ++SL++  GE + LLGPSGCGKTT LR IAGLE   RG +Y
Sbjct: 8   AQIKVRNIHKRFGAFTALNDVSLDIAAGELVCLLGPSGCGKTTLLRCIAGLERQDRGTLY 67

Query: 62  IGDKLVADPEKGIFVPPKDRDIAMVFQSYALYPHMTVYDNIAFPLKLRKVPRQEIDQRVR 121
           IG++ ++D      + P+ RD  ++FQSYAL+P++TV  NIA+ L      R++  QRV 
Sbjct: 68  IGERDISD------LSPQARDYGILFQSYALFPNLTVEANIAYGLT--GSGREQARQRVA 119

Query: 122 EVAELLGLTELLNRKPRELSGGQRQRVALGRAIVRKPQVFLMDEPLSNLDAKLRVRMRAE 181
           E+ EL+GL+    + P +LSGGQ+QRVAL RA+   P + L+DEP+S LDA++R  +  E
Sbjct: 120 EMLELVGLSGSEKKYPGQLSGGQQQRVALARALAPSPSLLLLDEPMSALDARVREHLCTE 179

Query: 182 LKKLQRQLGVTTIYVTHDQVEAMTMGDRIAVMNRGVLQQVGSPDEVYDKPANTFVAGFIG 241
           L++LQRQLG+TT+ VTH+Q EAM M DRIAVMN G ++Q  +P E+YD PA  FVA F+G
Sbjct: 180 LRQLQRQLGITTLMVTHNQDEAMLMADRIAVMNNGQVEQYATPQEIYDHPATPFVAEFVG 239

Query: 242 SPPMNFLDAIVTEDGFVDFGEFRLKLLPDQFEVLGELGYVGREVIF---GIRPEDLYDAM 298
               N+L    + D     G+  ++L P   +      +   E I     +  E+L+ AM
Sbjct: 240 QG--NWLPFQRSSDSHALVGDMNMRLAPGSAQASSGRLFCRPEAITVNPVVHEENLFPAM 297

Query: 299 FAQVRVPGENLVRAVVEIVENLGSERIVHLRVGGVTFVGS 338
             ++   G N  R   E+    G   +  L    +  +GS
Sbjct: 298 VREITFLG-NRCRMSFELKALPGHALLAELAPEAMPRLGS 336


Lambda     K      H
   0.323    0.142    0.406 

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: 345
Number of extensions: 17
Number of successful extensions: 3
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: 372
Length of database: 352
Length adjustment: 29
Effective length of query: 343
Effective length of database: 323
Effective search space:   110789
Effective search space used:   110789
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.5 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.9 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