Aligments for a candidate for aacS in Pseudomonas putida KT2440

GapMind for catabolism of small carbon sources

Aligments for a candidate for aacS in Pseudomonas putida KT2440

Align Acetoacetate--CoA ligase (EC 6.2.1.16) (characterized)
to candidate PP_4550 PP_4550 long-chain-fatty-acid/CoA ligase

Query= reanno::acidovorax_3H11:Ac3H11_3009
         (578 letters)



>FitnessBrowser__Putida:PP_4550
          Length = 562

 Score =  243 bits (621), Expect = 1e-68
 Identities = 166/534 (31%), Positives = 258/534 (48%), Gaps = 43/534 (8%)

Query: 54  GRRYTYAQLQTEAHRLASALLG-MGLTPGDRVGIWSHNNAEWVLMQLATAQVGLVLVNIN 112
           G   +YA+L+  +   A+ L     L PG+R+ +   N  ++ +      + GL++VN N
Sbjct: 47  GVTLSYAELERHSAAFAAWLQQHTDLKPGERIAVQMPNVLQYPIAVFGAMRAGLIVVNTN 106

Query: 113 PAYRTAEVEYALNKVGCKLLVSMARFKTSDYLGMLRELAPEW------QGQQPGHLQAAK 166
           P Y   E+ +     G + LV +  F        ++E+ P+       + +    L AAK
Sbjct: 107 PLYTEREMRHQFKDSGARALVYLNMFGKR-----VQEVLPDTGIEYLIEAKMGDLLPAAK 161

Query: 167 LPQLKTVVWIDDEAGQGADEPGLLRFTELIARGNAADPRLAQVAAGLQATDPINIQFTSG 226
              + TVV    +       P  + F +++  G    P+       L   D   +Q+T G
Sbjct: 162 GWLVNTVVDKLKKMVPAYRLPQAVPFKQVLREGRGLSPK----PVSLNLDDIAVLQYTGG 217

Query: 227 TTGFPKGATLTHRNILNNGFFIGECMKLTPADR----------LCIPVPLYHCFGMVLGN 276
           TTG  KGA LTH N++ N   +  C      D           +  P+PLYH +     N
Sbjct: 218 TTGLAKGAMLTHGNLVANMLQVLACFSQHGPDGQKLLKDGQEVMIAPLPLYHIYAFT-AN 276

Query: 277 LACF----THGATIVYPND--GFDPLTVLQTVQDERCTGLHGVPTMFIAELDHPRFAEFN 330
             C      H   I  P D  GF     ++ +   R + L G+ T+F+A +DHP F + +
Sbjct: 277 CMCMMVTGNHNVLITNPRDIPGF-----IKELGKWRFSALLGLNTLFVALMDHPGFRQLD 331

Query: 331 LSTLRTGIMAGSPCPTEVMKRVVEQMNLREITIAYGMTETSPVSCQSSTDTPLSKRVSTV 390
            S L+     G+       +R  +    R I   YG+TETSPV+  S+       R+ TV
Sbjct: 332 FSALKVTNSGGTALVKATAERWEDLTGCR-IVEGYGLTETSPVA--STNPYGQLARLGTV 388

Query: 391 GQVQPHLEVKIVDPDTGAVVPIGQRGEFCTKGYSVMHGYWGDEAKTREAIDEGGWMHTGD 450
           G        K++D D G  +P+G+RGE C KG  VM GYW     T +A+D  GW  TGD
Sbjct: 389 GIPVAGTAFKVIDDD-GNELPLGERGELCIKGPQVMKGYWQQPEATAQALDAEGWFKTGD 447

Query: 451 LATMDAEGYVNIVGRIKDMVIRGGENIYPREIEEFLYRHPQVQDVQVVGVPDQKYGEELC 510
           +A +D +G+  IV R KDM+I  G N+YP EIE+ +  HP+V +   +GVPD++ GE + 
Sbjct: 448 IAVIDPDGFTRIVDRKKDMIIVSGFNVYPNEIEDVVMGHPKVANCAAIGVPDERSGEAVK 507

Query: 511 AWIIAKPGTQPTEDDIRAFCKGQIAHYKVPRYIRFVTSFPMTVTGKIQKFKIRD 564
            +++ + G   + D+++A+CK     YKVP++I    S PMT  GKI + ++RD
Sbjct: 508 LFVVPREGGL-SVDELKAYCKANFTGYKVPKHIVLRESLPMTPVGKILRRELRD 560


Lambda     K      H
   0.320    0.136    0.412 

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: 787
Number of extensions: 46
Number of successful extensions: 6
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: 578
Length of database: 562
Length adjustment: 36
Effective length of query: 542
Effective length of database: 526
Effective search space:   285092
Effective search space used:   285092
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: 53 (25.0 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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Protein sequences (fasta format)
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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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

GapMind for catabolism of small carbon sources