GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK in Caulobacter crescentus NA1000

Align MsmK aka SMU.882, component of The raffinose/stachyose transporter, MsmEFGK (MalK (3.A.1.1.27) can probably substitute for MsmK; Webb et al., 2008). This system may also transport melibiose, isomaltotriose and sucrose as well as isomaltosaccharides (characterized)
to candidate CCNA_01670 CCNA_01670 sulfate transport ATP-binding protein cysA

Query= TCDB::Q00752
         (377 letters)



>FitnessBrowser__Caulo:CCNA_01670
          Length = 339

 Score =  191 bits (485), Expect = 3e-53
 Identities = 113/292 (38%), Positives = 163/292 (55%), Gaps = 31/292 (10%)

Query: 10  YKKYPNSSHYSVEDFDLDIKNKEFIVFVGPSGCGKSTTLRMVAGLEDITKGELKIDGEVV 69
           + +YP     ++   DL+I + E +  +GPSG GK+T LR +AGLE    G++  DG+ V
Sbjct: 12  FGRYP-----ALNKVDLEIADGELLALLGPSGSGKTTLLRTIAGLEFPDAGQVLFDGQDV 66

Query: 70  NDKAPKDRDIAMVFQNYALYPHMSVYDNMAFGLKLRHY----SKEAIDKRVKEAAQILGL 125
              +   R +  VFQ YAL+ HM+V  N+AFGL +R      SK  I +RV+E  +++ L
Sbjct: 67  TYASAAARRVGFVFQQYALFKHMTVAKNIAFGLDVRKGKDKPSKAEIARRVEELLKLVEL 126

Query: 126 TEFLERKPADLSGGQRQRVAMGRAIVRDAKVFLMDEPLSNLDAKLRVSMRAEIAKIHRRI 185
                R P+ LSGGQRQRVA+ RA+     V L+DEP   LDA +R S+R E+ ++H   
Sbjct: 127 EGLGGRYPSQLSGGQRQRVALSRALAVQPSVLLLDEPFGALDATVRKSLRRELRRVHDAT 186

Query: 186 GATTIYVTHDQTEAMTLADRIVIMSSTKNEDGSGTIGRVEQVGTPQELYNRPANKFVAGF 245
           G TTI+VTHDQ EA+ LADR+ I+++          GR+EQ+GTP ++++ P   FV GF
Sbjct: 187 GVTTIFVTHDQEEALELADRVAILNN----------GRIEQIGTPDQVHDAPETAFVCGF 236

Query: 246 IGSPAMNFFDVTIKDGHLVS----------KDGLTIAVTEGQLKMLESKGFK 287
           +G    N FD  +  G   +          KDG   A        L+  GF+
Sbjct: 237 VGE--ANRFDGQVSGGRFKAGALTVPASALKDGAATAYVRPHDFALDEAGFE 286


Lambda     K      H
   0.318    0.135    0.375 

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: 328
Number of extensions: 14
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: 339
Length adjustment: 29
Effective length of query: 348
Effective length of database: 310
Effective search space:   107880
Effective search space used:   107880
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