GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Methylobacterium sp. 4-46

Align Short-chain acyl-CoA dehydrogenase (EC 1.3.8.1) (characterized)
to candidate WP_012333698.1 M446_RS18850 acyl-CoA dehydrogenase

Query= reanno::pseudo13_GW456_L13:PfGW456L13_2983
         (375 letters)



>NCBI__GCF_000019365.1:WP_012333698.1
          Length = 376

 Score =  518 bits (1335), Expect = e-152
 Identities = 263/372 (70%), Positives = 307/372 (82%)

Query: 4   NDDQQQIRDMARDFAQERLKPFAAEWDREHRFPKEAIGEMAGLGFFGMLVPEQWGGCDTG 63
           +DDQ  IRD AR FAQ RL+PFAAEWDR+ RFP+EA+  +  LGF GMLVPE +GG    
Sbjct: 3   SDDQILIRDTARSFAQARLRPFAAEWDRDSRFPREAVAALGELGFLGMLVPEAYGGSAVD 62

Query: 64  YLAYAMALEEIAAGDGACSTIMSVHNSVGCVPILNYGTDEQKERFLKPLASGAMLGAFAL 123
           +++YA+A+EEIAAGDGA STIMSVHNSV CVPIL +GT+ QKERFL PLA GA LGAF L
Sbjct: 63  HVSYALAIEEIAAGDGAVSTIMSVHNSVACVPILRFGTEAQKERFLVPLARGAQLGAFCL 122

Query: 124 TEPQAGSDASGLKTRARLEGDHYVLNGCKQFITSGQNAGVVIVFAVTDPSAGKRGISAFI 183
           TEP AGSDA  +  RAR  G+ YVL+G KQFITSG++A + IVFAVTDP AGKRGISAFI
Sbjct: 123 TEPGAGSDAGAVTARARRVGNRYVLSGTKQFITSGRSADLAIVFAVTDPEAGKRGISAFI 182

Query: 184 VPTDSPGYKVARVEDKLGQHASDTCQILFEDVKVPLANRLGEEGEGYRIALANLEGGRVG 243
           VPT +PGY+VAR+E KLGQ ASDT QI+FED+++     LG+EGEG RIAL+NLEGGR+G
Sbjct: 183 VPTATPGYRVARIEHKLGQRASDTAQIVFEDMELTPDLLLGQEGEGLRIALSNLEGGRIG 242

Query: 244 IASQSVGMARAAFEAARDYARERESFGKPIIEHQAVAFRLADMATQIAVARQMVHYAAAL 303
           IA+Q+VGMARAAFEAA  YA ERE+FG+ +  HQAVAFRLADMAT+I  AR +VH AA L
Sbjct: 243 IAAQAVGMARAAFEAALAYAGERETFGQKLTAHQAVAFRLADMATRIEAARLLVHNAARL 302

Query: 304 RDSGKPALVEASMAKLFASEMAEKVCSSALQTLGGYGYLNDFPVERIYRDVRVCQIYEGT 363
           RD+G+P L EA+MAKLFASEMAE VCS A+Q  GGYGYL D+PVERIYRDVRVCQIYEGT
Sbjct: 303 RDAGQPCLKEAAMAKLFASEMAEAVCSDAIQIHGGYGYLADYPVERIYRDVRVCQIYEGT 362

Query: 364 SDIQRMVISRNL 375
           SD+QR+VISR L
Sbjct: 363 SDVQRIVISRAL 374


Lambda     K      H
   0.320    0.135    0.394 

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: 459
Number of extensions: 16
Number of successful extensions: 1
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: 376
Length adjustment: 30
Effective length of query: 345
Effective length of database: 346
Effective search space:   119370
Effective search space used:   119370
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 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