GapMind for catabolism of small carbon sources

 

Alignments for a candidate for L-LDH in Cupriavidus basilensis 4G11

Align L-lactate dehydrogenase; EC 1.1.1.27 (uncharacterized)
to candidate RR42_RS29130 RR42_RS29130 dehydrogenase

Query= curated2:Q07251
         (349 letters)



>FitnessBrowser__Cup4G11:RR42_RS29130
          Length = 364

 Score =  228 bits (581), Expect = 2e-64
 Identities = 133/348 (38%), Positives = 189/348 (54%), Gaps = 6/348 (1%)

Query: 2   KISLTSARQLARDILAAQQVPADIADDVAEHLVESDRCGYISHGLSILPNYRTALDGHSV 61
           +I   +  Q   D+  A    A  A   A+HLV ++  G+ SHG+ ++P Y  +  G  +
Sbjct: 5   RIPTPALHQWVVDLWRAAGSDAREARLTADHLVGANLSGHDSHGVGMIPKYVMSWQGEQL 64

Query: 62  NPQGRAKCVLDQGTLMVFDGDGGFGQHVGKSVMQAAIERVRQHGHCIVTLRRSHHLGRMG 121
               R   V + G ++  DG+ G GQ V +  M  AIER R+HG C++ LR SHHLGR+G
Sbjct: 65  QLNQRVSVVHEAGGILSLDGNRGMGQAVTEEAMGLAIERAREHGVCVLGLRASHHLGRVG 124

Query: 122 HYGEMAAAAGFVLLSFTNVINRAPVVAPFGGRVARLTTNPLCFAGPMPNGRPPLVVDIAT 181
           H+ E A AAG + + F NV+++ P+VAP GG  AR  TNP     P+  G  PLV+D AT
Sbjct: 125 HWAEQATAAGMISIHFVNVLSK-PIVAPHGGYEARYGTNPFTIGVPVAGGE-PLVMDFAT 182

Query: 182 SAIAINKARVLAEKGEPAPEGSIIGADGNPTTDASTMF---GEHPGALLPFGGHKGYALG 238
           SAIA+ K RV   KG   P G ++  +G+PT D + MF   GE  GAL PFG HKGY L 
Sbjct: 183 SAIALGKVRVANNKGVAVPPGCLLDTEGHPTDDPAVMFPPAGEAQGALRPFGEHKGYVLA 242

Query: 239 VVAELLAGVLSGGGTIQPDN-PRGGVATNNLFAVLLNPALDLGLDWQSAEVEAFVRYLHD 297
           V+ ELL   ++GG TI+P+         NN+ A++ +P           EV+AFV +L  
Sbjct: 243 VMCELLGAAVTGGHTIRPETLTHEHAVWNNMLAIVFDPERLGSSTTFGHEVQAFVDWLRS 302

Query: 298 TPPAPGVDRVQYPGEYEAANRAQASDTLNINPAIWRNLERLAQSLNVA 345
           +   PG D +  PGE E A R   ++ + ++      L+  A  +  A
Sbjct: 303 SHLQPGTDAILLPGEPERAWRRARAEFMPVDSGTLAQLDDAAARVQAA 350


Lambda     K      H
   0.319    0.136    0.409 

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: 444
Number of extensions: 25
Number of successful extensions: 6
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: 349
Length of database: 364
Length adjustment: 29
Effective length of query: 320
Effective length of database: 335
Effective search space:   107200
Effective search space used:   107200
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 (21.7 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