GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acdH in Cupriavidus basilensis 4G11

Align Short-chain acyl-CoA dehydrogenase (EC 1.3.8.1) (characterized)
to candidate RR42_RS28565 RR42_RS28565 acyl-CoA dehydrogenase

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



>FitnessBrowser__Cup4G11:RR42_RS28565
          Length = 377

 Score =  468 bits (1203), Expect = e-136
 Identities = 232/372 (62%), Positives = 287/372 (77%)

Query: 4   NDDQQQIRDMARDFAQERLKPFAAEWDREHRFPKEAIGEMAGLGFFGMLVPEQWGGCDTG 63
           ++ Q  IRD AR FA ERL P AAEWDR  + P E + EM  LG  GM+VPE+WGG  T 
Sbjct: 6   SEQQTMIRDTARTFASERLAPCAAEWDRAGQLPAEVVAEMGALGLLGMIVPEEWGGTYTD 65

Query: 64  YLAYAMALEEIAAGDGACSTIMSVHNSVGCVPILNYGTDEQKERFLKPLASGAMLGAFAL 123
           Y+AYA+A+EEIAAG  AC+T+MSVHNSVGC PIL+YGT  QKER+L  LASG ++GAF L
Sbjct: 66  YIAYALAIEEIAAGCAACATLMSVHNSVGCGPILHYGTQAQKERYLPRLASGEIIGAFCL 125

Query: 124 TEPQAGSDASGLKTRARLEGDHYVLNGCKQFITSGQNAGVVIVFAVTDPSAGKRGISAFI 183
           TEPQAGS+A  L+TRAR   + +VL+G KQF+T+GQ AGV IVFA T+P+ GKRG+SAF+
Sbjct: 126 TEPQAGSEAHNLRTRARATDNGWVLSGSKQFVTNGQRAGVAIVFAATEPAQGKRGLSAFV 185

Query: 184 VPTDSPGYKVARVEDKLGQHASDTCQILFEDVKVPLANRLGEEGEGYRIALANLEGGRVG 243
           VPTD+PG+ V   E K+G  ASDTC I  +D +VP    LGE GEG RIAL+NLEGGR+G
Sbjct: 186 VPTDTPGFSVHTPERKMGIRASDTCAITLDDCQVPHDALLGEPGEGLRIALSNLEGGRIG 245

Query: 244 IASQSVGMARAAFEAARDYARERESFGKPIIEHQAVAFRLADMATQIAVARQMVHYAAAL 303
           IA+Q++G+AR+AFEAA  YA ER  FG+P+ EH  +A  LADMAT++  AR +VH AA +
Sbjct: 246 IAAQALGIARSAFEAACRYAAERVQFGRPLREHAPIANMLADMATELNAARLLVHRAAHM 305

Query: 304 RDSGKPALVEASMAKLFASEMAEKVCSSALQTLGGYGYLNDFPVERIYRDVRVCQIYEGT 363
           R +G+P L EAS AKL+ASE+AE+VCS ALQ  GGYGYL D+PVER YRD R+ QIYEGT
Sbjct: 306 RTAGQPCLSEASQAKLYASELAERVCSKALQIHGGYGYLEDYPVERHYRDARITQIYEGT 365

Query: 364 SDIQRMVISRNL 375
           S+IQRM+I+R L
Sbjct: 366 SEIQRMLIARTL 377


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: 419
Number of extensions: 10
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: 377
Length adjustment: 30
Effective length of query: 345
Effective length of database: 347
Effective search space:   119715
Effective search space used:   119715
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