GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dhaD in Herbaspirillum seropedicae SmR1

Align alcohol dehydrogenase (EC 1.1.1.1); long-chain-alcohol dehydrogenase (EC 1.1.1.192) (characterized)
to candidate HSERO_RS00730 HSERO_RS00730 4-hydroxybutyrate dehydrogenase

Query= BRENDA::A4IP64
         (395 letters)



>FitnessBrowser__HerbieS:HSERO_RS00730
          Length = 379

 Score =  181 bits (459), Expect = 3e-50
 Identities = 120/351 (34%), Positives = 192/351 (54%), Gaps = 17/351 (4%)

Query: 16  WGALDQLVPEVKRLGAKHILVITDPMLVKIGLVDQVTSPLRQEGYSVHVYTDVVPEPPLE 75
           +GAL  L  E  RLG K  LV+TD  +   GL+D+V   L+ EG    VY    P P   
Sbjct: 14  YGALALLQQECDRLGIKKPLVVTDMGIRNAGLLDKVLGQLK-EGVGAVVYDQTPPNPNEG 72

Query: 76  TGEKAVAFARDGKFDLVIGVGGGSALDLAKLAAVLAVHDGSVADYLNLTG-TRTLEKKGL 134
               AVA  R    D ++ VGGGS++DLAK  AV   H+G +  +  + G    +  K  
Sbjct: 73  AVRAAVALFRQHGCDGIVAVGGGSSIDLAKGVAVCGTHEGPLKSFALIEGGLANITAKTA 132

Query: 135 PKILIPTTSGTGSEVTNISVLSLETTKDV-VTHDYLLADVAIVDPQLTVSVPPRVTAATG 193
           P I IPTT+GTGSEV   ++L L+  + V +   YL+  +AI DP+LT+ +PP +TAATG
Sbjct: 133 PVIAIPTTAGTGSEVGRGAILILDDGRKVGIISPYLVPKLAICDPELTLGLPPLMTAATG 192

Query: 194 IDALTHAVEAYVSVNASPTSDGLAVAAIRLISRSLRKAVANGSDKQARIDMANGSYLAGL 253
           +DA+ H +E +++ + +P +DG+A+  +      + +A     D++AR++M + S + G 
Sbjct: 193 MDAIAHCLETFMAPSFNPPADGIALDGLWRAWAHIERATREPGDREARLNMMSAS-MQGA 251

Query: 254 AFFNAGVAGVHALAYPLGG-QFHIAHGESNAVLLPYVMGYIRQSCT----KRMADIFNAL 308
             F  G+  VH+L++ LGG    + HG  NA+ LP ++ +   + +     +MA + +A+
Sbjct: 252 MAFQKGLGCVHSLSHSLGGINPRLHHGTLNAIFLPAIIAFNESAASMVKDNKMARMAHAM 311

Query: 309 GGNSSFLSEVEASYRCVEELERFVADVGIPKTLGGFGIPESALESLTKDAV 359
           G  S   +E+  + R   E+ R    +G+P  LG  G+ ES    + + A+
Sbjct: 312 GLGSG--AEIGPAIR---EMSR---RLGLPAGLGELGVTESMFPQIIQGAL 354


Lambda     K      H
   0.318    0.135    0.381 

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: 384
Number of extensions: 25
Number of successful extensions: 5
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: 395
Length of database: 379
Length adjustment: 30
Effective length of query: 365
Effective length of database: 349
Effective search space:   127385
Effective search space used:   127385
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 50 (23.9 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