GapMind for catabolism of small carbon sources

 

Alignments for a candidate for L-LDH in Paraburkholderia bryophila 376MFSha3.1

Align L-lactate dehydrogenase; EC 1.1.1.27 (uncharacterized)
to candidate H281DRAFT_05436 H281DRAFT_05436 Malate/lactate/ureidoglycolate dehydrogenase, LDH2 family

Query= curated2:Q07251
         (349 letters)



>FitnessBrowser__Burk376:H281DRAFT_05436
          Length = 330

 Score =  139 bits (351), Expect = 8e-38
 Identities = 98/327 (29%), Positives = 164/327 (50%), Gaps = 14/327 (4%)

Query: 29  VAEHLVESDRCGYISHGLSILPNYRTALDGHSVNPQGRAKCVLDQGTLMVFDGDGGFGQH 88
           VA  LV+ D  G+ +HGL++LP Y   ++  ++   G  + V D+G  +++DG    G  
Sbjct: 9   VARTLVDGDLMGHDTHGLALLPAYIGEIENGAMTCSGEPEVVSDRGGSVLWDGRRLPGPW 68

Query: 89  VGKSVMQAAIERVRQHGHCIVTLRRSHHLGRMGHYGEMAAAAGF-VLLSFTNVINRAPVV 147
           +  S ++    R +++G   + +RRSHH+  +  Y E A A GF +LLS ++   ++  V
Sbjct: 69  LVLSGIETLAPRAKKYGTATLVIRRSHHIACLASYLERATADGFMILLSSSDPAGQS--V 126

Query: 148 APFGGRVARLTTNPLCFAGPMPNGRPPLVVDIATSAIAINKARVLAEKGEPAPEGSIIGA 207
           AP GG  +  T NP+  A  +P    P ++DI++S +         + G+   E   + A
Sbjct: 127 APHGGTRSVFTPNPI--AAGIPTSGSPFLIDISSSMVTQGMTARRHKAGQHFEEACFLDA 184

Query: 208 DGNPTTDASTMFGEHPGALLPF----GGHKGYALGVVAELLAGVLSGGGTIQPDNPRGGV 263
           DG P+ D S +  + PG++LP     GGHKG+ L ++ E L G L+G G   P +  GG 
Sbjct: 185 DGQPSGDPSVLCTDPPGSILPIGGMTGGHKGFGLALLIEALTGGLAGHGRADPADGWGG- 243

Query: 264 ATNNLFAVLLNPALDLGLDWQSAEVEAFVRYLHDTPPAPGVDRVQYPGEYEA-ANRAQAS 322
               +F  L + A   GL     +++       + PP PG   V+ PG+      R Q  
Sbjct: 244 ---TVFLSLYDTAAFGGLAAFVRQMDWLGDACRNNPPRPGTAGVRMPGDRGLNLKREQLR 300

Query: 323 DTLNINPAIWRNLERLAQSLNVAVPTA 349
           D + ++  I   LE  A+  ++ +P+A
Sbjct: 301 DGVALHSTIAPALEACARRYDIPLPSA 327


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: 380
Number of extensions: 22
Number of successful extensions: 4
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: 330
Length adjustment: 28
Effective length of query: 321
Effective length of database: 302
Effective search space:    96942
Effective search space used:    96942
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