GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdh in Beijerinckia indica ATCC 9039

Align L-iditol 2-dehydrogenase (EC 1.1.1.14); D-xylulose reductase (EC 1.1.1.9) (characterized)
to candidate WP_012385307.1 BIND_RS11835 NAD(P)-dependent alcohol dehydrogenase

Query= reanno::HerbieS:HSERO_RS17015
         (345 letters)



>NCBI__GCF_000019845.1:WP_012385307.1
          Length = 348

 Score =  441 bits (1133), Expect = e-128
 Identities = 218/343 (63%), Positives = 267/343 (77%)

Query: 1   MQALVLEATRELKLREIDLPQQMGAQDVRIRIHTVGICGSDLHYYTHGSIGPFKVEAPMV 60
           MQALVLE   EL LR++DLP  +G   V+I +HTVGICGSD+HY+THGSIGP+ VE PMV
Sbjct: 1   MQALVLERKGELSLRDVDLPLAVGPGQVKIAVHTVGICGSDVHYFTHGSIGPYIVEKPMV 60

Query: 61  LGHEASGTVIEVGSAVSHLKVGDRVCMEPGIPRLDSPATLRGMYNLDPAVRFWATPPIHG 120
           LGHEA+GT++EVG  VS LKVGDRVCMEPG+P + S A+  G+YN+DP+V FWATPP+HG
Sbjct: 61  LGHEATGTIVEVGPNVSTLKVGDRVCMEPGVPDMSSRASKLGLYNVDPSVTFWATPPVHG 120

Query: 121 CLTGSVVHPAAFTYRLPDNVSFAEGAIVEPLSIGLQAATKARMKPGDTAVVIGAGTIGAM 180
            LT  VVHPAAFTY+LP NVSFAEGA+VEP +IG+QAAT+AR+ PGD A VIGAGTIG M
Sbjct: 121 VLTPYVVHPAAFTYKLPANVSFAEGALVEPFAIGMQAATRARIAPGDVAAVIGAGTIGIM 180

Query: 181 TALAALAGGAARVILADVVAEKLAHFADNPAVITVDVTRETLTDVVRQATDGWGADVVFE 240
           TALAA+AGG +RV ++D   EKLA       ++ V+   E+L DVV + T+ WGADVVFE
Sbjct: 181 TALAAVAGGCSRVFISDFSKEKLAIAGGYDCIVPVNAGEESLADVVARETENWGADVVFE 240

Query: 241 ASGHAGVYQTLLDLVCPGGCAVLVGMPPAPVALDVVAMQTKEVRLESVFRYANIFPRALA 300
           ASG    Y  L  +V PGG  VLVG+P  PVA DV +  +KEVR+E+VFRYANIF RALA
Sbjct: 241 ASGSPKAYGDLFRIVRPGGAVVLVGLPVEPVAFDVSSAISKEVRIETVFRYANIFDRALA 300

Query: 301 LISSGMIDVKPFISRKFPFSQSIRAFEEAASGRPQDVKIQIEM 343
           LI+SG +++KP I+  FPFS S+ AFE AA+GRP DVK+QIE+
Sbjct: 301 LIASGKVNLKPLITGTFPFSDSVVAFERAAAGRPTDVKLQIEV 343


Lambda     K      H
   0.321    0.137    0.403 

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: 407
Number of extensions: 12
Number of successful extensions: 1
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: 345
Length of database: 348
Length adjustment: 29
Effective length of query: 316
Effective length of database: 319
Effective search space:   100804
Effective search space used:   100804
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 (21.9 bits)
S2: 49 (23.5 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