GapMind for catabolism of small carbon sources

 

Alignments for a candidate for L-LDH in Xenophilus azovorans DSM 13620

Align L-lactate dehydrogenase; EC 1.1.1.27 (uncharacterized)
to candidate WP_038216210.1 Q392_RS27395 malate/lactate/ureidoglycolate dehydrogenase

Query= curated2:Q07251
         (349 letters)



>NCBI__GCF_000745855.1:WP_038216210.1
          Length = 378

 Score =  237 bits (605), Expect = 3e-67
 Identities = 154/372 (41%), Positives = 191/372 (51%), Gaps = 40/372 (10%)

Query: 11  LARDILAAQQVPADIADDVAEHLVESDRCGYISHGLSILPNYRTALDGHSVNPQGRAKCV 70
           +AR I AA    A+ A  VA +LV ++  G+ SHG+ ++P Y  A+    + P   AK  
Sbjct: 11  VARVIAAAGSAEAE-AQTVAANLVLANLSGHDSHGVGMVPRYVDAVQEGGLKPNTGAKVT 69

Query: 71  LDQGTLMVFDGDGGFGQHVGKSVMQAAIERVRQHGHCIVTLRRSHHLGRMGHYGEMAAAA 130
           LD GTL+  DG  G+GQ VG+  MQ  IER  QHG CI+T+  SHH+GR+GH+ EMA AA
Sbjct: 70  LDIGTLLALDGQRGYGQVVGEQAMQMGIERALQHGSCILTVGNSHHMGRIGHFAEMAVAA 129

Query: 131 GFVLLSFTNVINRAPVVAPFGGRVARLTTNPLCF-----------AGPMPNGRPP----- 174
           G V L F NV++R PVVAPFGG   R  TNP C            AGP   G  P     
Sbjct: 130 GLVSLHFVNVLSR-PVVAPFGGGDGRFGTNPCCIGVPLKRQERSAAGPPQGGAAPPGGSD 188

Query: 175 -----------LVVDIATSAIAINKARVLAEKGEPAPEGSIIGADGNPTTDASTMF---- 219
                       V+D ATS +A  K RV   KGE  PEG +I   G PTTD   +     
Sbjct: 189 PHAVGERGGEHFVLDFATSRVAQGKMRVAHNKGEQVPEGYLIDERGAPTTDPGVVVVPQA 248

Query: 220 GEHPGALLPFGGHKGYALGVVAELLAGVLSGGGTIQPDNPRGGVATNNLFAVLLNPALDL 279
           G   GAL+ FG HKGY + V  ELL G LSGGGT            N +  VL++PA   
Sbjct: 249 GGLFGALMTFGEHKGYGMAVACELLGGALSGGGTWHRAPDAARTVLNGMLTVLIDPA--- 305

Query: 280 GLDWQSA---EVEAFVRYLHDTPPAPGVDRVQYPGEYE-AANRAQASDTLNINPAIWRNL 335
            L  Q A   E  AFV +L   PP  G + VQ  GE E  A  A+  D + I+ A W  L
Sbjct: 306 RLGTQQAFEQEAAAFVDWLRQCPPGAGFEGVQIAGEPERRARAARGRDGIAIDDATWAEL 365

Query: 336 ERLAQSLNVAVP 347
                 + VA+P
Sbjct: 366 HAAGAKVGVALP 377


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: 396
Number of extensions: 31
Number of successful extensions: 7
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: 378
Length adjustment: 29
Effective length of query: 320
Effective length of database: 349
Effective search space:   111680
Effective search space used:   111680
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 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