GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sdh in Rhizobium leguminosarum 3841

Align L-iditol 2-dehydrogenase (EC 1.1.1.14); D-xylulose reductase (EC 1.1.1.9) (characterized)
to candidate WP_011655124.1 RL_RS31695 NAD(P)-dependent alcohol dehydrogenase

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



>NCBI__GCF_000009265.1:WP_011655124.1
          Length = 347

 Score =  434 bits (1115), Expect = e-126
 Identities = 210/344 (61%), Positives = 263/344 (76%)

Query: 1   MQALVLEATRELKLREIDLPQQMGAQDVRIRIHTVGICGSDLHYYTHGSIGPFKVEAPMV 60
           ++ALVLE   EL LR+IDLP + G  +V+IRIHTVG+CGSD+HYYTHG IGPF V APMV
Sbjct: 4   VRALVLERQHELALRDIDLPLETGPGEVKIRIHTVGVCGSDVHYYTHGKIGPFVVNAPMV 63

Query: 61  LGHEASGTVIEVGSAVSHLKVGDRVCMEPGIPRLDSPATLRGMYNLDPAVRFWATPPIHG 120
           LGHEA+GTV+EVG+ V+HLKVGDRVCMEPGIP  +S A+  GMYN+DPAV FWATPPIHG
Sbjct: 64  LGHEAAGTVVEVGAGVTHLKVGDRVCMEPGIPDPNSKASRLGMYNIDPAVTFWATPPIHG 123

Query: 121 CLTGSVVHPAAFTYRLPDNVSFAEGAIVEPLSIGLQAATKARMKPGDTAVVIGAGTIGAM 180
            LT  VVHPA +T++LPDNVSFAEGA+VEP ++G+QAATKA++ PGDTAVV+GAG IG M
Sbjct: 124 VLTPEVVHPANYTFKLPDNVSFAEGAMVEPFAVGMQAATKAKITPGDTAVVLGAGPIGTM 183

Query: 181 TALAALAGGAARVILADVVAEKLAHFADNPAVITVDVTRETLTDVVRQATDGWGADVVFE 240
            A+AALAGG AR I+AD+   KL   A    VI V++  + L + V + TDGWGADVVFE
Sbjct: 184 VAIAALAGGCARAIVADLAQPKLDIAAQYQGVIPVNIREKNLAEEVARLTDGWGADVVFE 243

Query: 241 ASGHAGVYQTLLDLVCPGGCAVLVGMPPAPVALDVVAMQTKEVRLESVFRYANIFPRALA 300
            SG    ++T++ L  PGG  V+VG+P  P+  DV    TKE+R+E+VFRYA+ + R++A
Sbjct: 244 CSGSPKAWETIMALPRPGGVIVVVGLPVNPIGFDVSTASTKEIRIETVFRYAHQYERSIA 303

Query: 301 LISSGMIDVKPFISRKFPFSQSIRAFEEAASGRPQDVKIQIEME 344
           L+ SG +D+KP IS  F F  SI+AF+ A   RP DVK+QI ME
Sbjct: 304 LLGSGRVDLKPLISETFKFDDSIKAFDRAVEARPSDVKLQIVME 347


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: 372
Number of extensions: 11
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: 347
Length adjustment: 29
Effective length of query: 316
Effective length of database: 318
Effective search space:   100488
Effective search space used:   100488
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