GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Caulobacter crescentus NA1000

Align short-chain acyl-CoA dehydrogenase monomer (EC 1.3.8.1) (characterized)
to candidate CCNA_00436 CCNA_00436 acyl-CoA dehydrogenase, short-chain specific

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



>FitnessBrowser__Caulo:CCNA_00436
          Length = 382

 Score =  310 bits (795), Expect = 3e-89
 Identities = 157/370 (42%), Positives = 240/370 (64%), Gaps = 1/370 (0%)

Query: 5   DEQQQIADAVRAFAQERLKPFAEQWDKDHRFPKEAIDEMAELGLFGMLVPEQWGGSDTGY 64
           + ++Q+ D V  F  ERL+P   Q  ++   P + I+EM  LGLFG+ +PE++GG     
Sbjct: 6   ETREQLIDTVARFVAERLRPIEAQVAENDAVPDDVIEEMKGLGLFGLTIPEEFGGLGLTM 65

Query: 65  VAYAMALEEIAAGDGACSTIMSVHNSVGCVPILRFGNEQQKEQFLTPLATGAMLGAFALT 124
              A+   E+     A  ++   +  +G   ++ FGN++QK ++L  +A+GA++ +FALT
Sbjct: 66  EEEALVAIELGRASPAFRSVFGTNVGIGSQGLVMFGNDEQKAKWLPGIASGAVITSFALT 125

Query: 125 EPQAGSDASSLKTRARLEGDHYVLNGSKQFITSGQNAGVVIVFAVTDPEA-GKRGISAFI 183
           EP+AGSD+++++TRA  +GD Y+LNGSK++IT+   A +  V A T+P+A G  G+SAF+
Sbjct: 126 EPEAGSDSAAVQTRATRDGDDYILNGSKRYITNAGKASLFTVMARTNPDAKGGAGVSAFL 185

Query: 184 VPTDSPGYQVARVEDKLGQHASDTCQIVFDNVQVPVANRLGAEGEGYKIALANLEGGRIG 243
           VP D PG  V + E K+GQ  +    + FDNV+VP  NRLGAEGEG+K+A+  L+ GR+ 
Sbjct: 186 VPRDLPGLTVGKPEKKMGQQGAHIHDVTFDNVRVPAWNRLGAEGEGFKVAMQVLDRGRLH 245

Query: 244 IASQAVGMARAAFEVARDYANERQSFGKPLIEHQAVAFRLADMATKISVARQMVLHAAAL 303
           IA+  VG+A         YA+ER+ FG+P+   Q +   +AD  T+   A+ +VL  A  
Sbjct: 246 IAAVCVGVAERLIADCVAYASERKQFGQPIASFQLIQAMIADSKTEALAAKALVLETARK 305

Query: 304 RDAGRPALVEASMAKLFASEMAEKVCSDALQTLGGYGYLSDFPLERIYRDVRVCQIYEGT 363
           RDAG    +EA+ +KLFASEM  +V   A+Q  GG GY++D+ +ER+YRDVR+ +IYEGT
Sbjct: 306 RDAGVNVTLEAASSKLFASEMVGRVADRAVQVFGGAGYVADYGIERLYRDVRIFRIYEGT 365

Query: 364 SDIQRMVIAR 373
           S +Q+++IAR
Sbjct: 366 SQVQQLIIAR 375


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: 372
Number of extensions: 12
Number of successful extensions: 3
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: 382
Length adjustment: 30
Effective length of query: 345
Effective length of database: 352
Effective search space:   121440
Effective search space used:   121440
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 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