GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK in Cupriavidus basilensis 4G11

Align ABC-type maltose transporter (subunit 3/3) (EC 7.5.2.1) (characterized)
to candidate RR42_RS12955 RR42_RS12955 glycerol-3-phosphate ABC transporter ATP-binding protein

Query= BRENDA::P68187
         (371 letters)



>FitnessBrowser__Cup4G11:RR42_RS12955
          Length = 367

 Score =  333 bits (855), Expect = 3e-96
 Identities = 183/363 (50%), Positives = 242/363 (66%), Gaps = 8/363 (2%)

Query: 1   MASVQLQNVTKAW-GEVVVSKDINLDIHEGEFVVFVGPSGCGKSTLLRMIAGLETITSGD 59
           MA + L+NV K + G V V   I+++I++GEF+V VGPSGCGKSTLLRM+AGLE I+ G+
Sbjct: 1   MAKLSLRNVQKTYAGNVKVVHGIDMEINDGEFIVIVGPSGCGKSTLLRMVAGLEAISGGE 60

Query: 60  LFIGEKRMNDTPPAERGVGMVFQSYALYPHLSVAENMSFGLKLAGAKKEVINQRVNQVAE 119
           + IG+K +N   PAER + MVFQ+YALYPH+SV +NM++GLK+ G  K  I QRV   A 
Sbjct: 61  VHIGDKVVNHLEPAERDIAMVFQNYALYPHMSVYDNMAYGLKIRGMDKSEIEQRVKHAAG 120

Query: 120 VLQLAHLLDRKPKALSGGQRQRVAIGRTLVAEPSVFLLDEPLSNLDAALRVQMRIEISRL 179
           +L+LA LL+RKP+ALSGGQRQRVA+GR +V EP+VFL DEPLSNLDA LRVQMR+E+  L
Sbjct: 121 ILELAPLLERKPRALSGGQRQRVAMGRAIVREPAVFLFDEPLSNLDAKLRVQMRLELKEL 180

Query: 180 HKRLGRTMIYVTHDQVEAMTLADKIVVLDAGRVAQVGKPLELYHYPADRFVAGFIGSPKM 239
           H+RL  T +YVTHDQVEAMTLAD+++VL+ G V Q+G PLE+Y  PA  FVA FIGSP M
Sbjct: 181 HRRLRTTSMYVTHDQVEAMTLADRMMVLNGGSVEQIGTPLEVYARPASTFVASFIGSPPM 240

Query: 240 NFLPVKVTATAIDQVQVELPMPNRQQVWLPVESRDVQVGANMS----LGIRPEHLLPSDI 295
           N +PV  T     + Q+ +      Q   P     + +G ++     LG+RPEH+ P   
Sbjct: 241 NLVPVTRTNGGQGEAQMRVEQKPGAQ-GAPATLGHLPMGLHLPERALLGLRPEHIEPCAA 299

Query: 296 ADVILEGEVQVVEQLGNETQIHIQIPSIRQNLVYRQNDVVLVEEGATFAIGLPPERCHLF 355
            + I E EV++VE LG ++  +  +    Q +V R +  + V  G    I    E  H F
Sbjct: 300 HEAIAEIEVRLVEALGADSYAYGTLGG--QPVVVRLDSNMPVSSGDRLPITAAAEHLHFF 357

Query: 356 RED 358
             D
Sbjct: 358 DAD 360


Lambda     K      H
   0.320    0.137    0.393 

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: 382
Number of extensions: 16
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: 371
Length of database: 367
Length adjustment: 30
Effective length of query: 341
Effective length of database: 337
Effective search space:   114917
Effective search space used:   114917
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 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