GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Sinorhizobium medicae WSM419

Align short-chain acyl-CoA dehydrogenase monomer (EC 1.3.8.1) (characterized)
to candidate WP_012061601.1 SMED_RS23355 acyl-CoA dehydrogenase

Query= metacyc::MONOMER-17424
         (375 letters)



>NCBI__GCF_000017145.1:WP_012061601.1
          Length = 395

 Score =  199 bits (507), Expect = 8e-56
 Identities = 127/372 (34%), Positives = 192/372 (51%), Gaps = 5/372 (1%)

Query: 3   VNDEQQQIADAVRAFAQERLKPFAEQWDKDHRFPKEAIDEMAELGLFGMLVPEQWGGSDT 62
           + ++++ I D  RA+AQE+L+P   +  ++         EM +LGL G+ VP+ +GG   
Sbjct: 19  LTEDERMIRDTARAYAQEKLQPRVIEAYREETTDPAIFREMGDLGLLGVTVPDSYGGVGA 78

Query: 63  GYVAYAMALEEIAAGDGACSTIMSVHNSVGCVPILRFGNEQQKEQFLTPLATGAMLGAFA 122
            YVAY +   E+   D    ++MSV +S+   PI  +G+E QK ++L  L +G  +G F 
Sbjct: 79  SYVAYGLVAREVERVDSGYRSMMSVQSSLVVYPIYAYGSEDQKRKYLPKLISGEWIGCFG 138

Query: 123 LTEPQAGSDASSLKTRA-RLEGDHYVLNGSKQFITSGQNAGVVIVFAVTDPEAGKRGISA 181
           LTEP AGSD + +KTRA R EG  Y L GSK +I++   A V +V+A +  EA    I  
Sbjct: 139 LTEPDAGSDPAGMKTRAIRTEGG-YRLIGSKMWISNAPLADVFVVWAKS--EAHDNAIRG 195

Query: 182 FIVPTDSPGYQVARVEDKLGQHASDTCQIVFDNVQVPVANRLGAEGEGYKIALANLEGGR 241
           F++   + G    ++  KL   AS T +IV DNV+V     L  + EG K     L   R
Sbjct: 196 FVLEKGTKGLSAPKIAGKLSLRASITGEIVLDNVEVG-EEALLPDVEGLKGPFGCLNRAR 254

Query: 242 IGIASQAVGMARAAFEVARDYANERQSFGKPLIEHQAVAFRLADMATKISVARQMVLHAA 301
            GI+  A+G A   +  AR Y  +R+ F +PL + Q    +LADM T+I++  Q  L   
Sbjct: 255 YGISWGALGAAEFCWHAARQYGLDRKQFNRPLAQTQLFQKKLADMQTEIALGLQGSLRVG 314

Query: 302 ALRDAGRPALVEASMAKLFASEMAEKVCSDALQTLGGYGYLSDFPLERIYRDVRVCQIYE 361
            L D GR A    S+ K      A  +   A    GG G   ++ + R   ++     YE
Sbjct: 315 RLMDEGRMAPEMISIVKRNNCGKALDIARQARDMHGGNGISEEYQVMRHMLNLETVNTYE 374

Query: 362 GTSDIQRMVIAR 373
           GT D+  +++ R
Sbjct: 375 GTHDVHALILGR 386


Lambda     K      H
   0.319    0.134    0.382 

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: 340
Number of extensions: 17
Number of successful extensions: 2
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: 375
Length of database: 395
Length adjustment: 30
Effective length of query: 345
Effective length of database: 365
Effective search space:   125925
Effective search space used:   125925
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: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. 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