GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dpkA in Cupriavidus basilensis 4G11

Align Delta(1)-pyrroline-2-carboxylate/Delta(1)-piperideine-2-carboxylate reductase; Pyr2C/Pip2C reductase; EC 1.5.1.1 (characterized)
to candidate RR42_RS20320 RR42_RS20320 ornithine cyclodeaminase

Query= SwissProt::V5YW53
         (311 letters)



>FitnessBrowser__Cup4G11:RR42_RS20320
          Length = 319

 Score =  174 bits (440), Expect = 3e-48
 Identities = 121/314 (38%), Positives = 163/314 (51%), Gaps = 27/314 (8%)

Query: 7   IPVFDAADTAALLAYPALLATLGQAVADYAAGEIVSPERLVVPL--QAGG--VMLSMPSS 62
           + + DAA TAA L YPAL   +   +A+  AG  ++P R+ +P+   AGG   +L MP+ 
Sbjct: 3   VALLDAAQTAARLPYPALARAIAAMLAELRAGTAMAPPRIALPVGDPAGGEGTLLVMPAR 62

Query: 63  ARDLATHKLVNVCPGNGARGLPTILGQVTAYDASTGEMRFALDGPTVTGRRTAAVTALGI 122
            R+L   K + V PGN  RGLP ILG+V   DA TG     LDGPTVTGRRTAAV+ L  
Sbjct: 63  NRELVMTKNITVHPGNPQRGLPNILGEVVVADAHTGRRLALLDGPTVTGRRTAAVSLLAA 122

Query: 123 QALHGAAPRDILLIGTGKQAANHAEALAAIFPEARLHVRGTSADSAAAFCAAHRAQAPRL 182
           Q+       ++L+IG G QA  H EA AA     R+ +   +A  A A  A  R      
Sbjct: 123 QSFAPDPAGELLIIGAGVQALTHLEAFAAGLSPRRVWLHSRTAAKAEALAAHARTLGVEA 182

Query: 183 VPLDG-DAIPDAIDVVVTLTTSRTPVYREAA----REGRLVVGVGAFTADAAEIDANTVR 237
             +D    +   + +VVT+T+S  PV  +      R+   +  VGAF  +  E+     +
Sbjct: 183 QSVDDVRTVLPRVSMVVTVTSSLVPVLPDLDSGLWRDDHFIAAVGAFRPEMCELPPALCQ 242

Query: 238 AS----RLVVDDPAGARHEAGDLIVAQVDWQHV-----ASLAD----VLGGTFDRSGPLL 284
           A+    RL+ D   G   EAGDL+ A + W  V     A LA+      GG+     PL+
Sbjct: 243 AASAHGRLLADTLFGIEEEAGDLLQAGIAWSTVQPFERAILAEDALRARGGS-----PLV 297

Query: 285 FKSVGCAAWDLAAC 298
           FKSVG A WDLAAC
Sbjct: 298 FKSVGYALWDLAAC 311


Lambda     K      H
   0.320    0.133    0.386 

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: 210
Number of extensions: 9
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: 311
Length of database: 319
Length adjustment: 27
Effective length of query: 284
Effective length of database: 292
Effective search space:    82928
Effective search space used:    82928
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: 48 (23.1 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