Aligments for a candidate for lat in Pseudomonas fluorescens GW456-L13

GapMind for catabolism of small carbon sources

Aligments for a candidate for lat in Pseudomonas fluorescens GW456-L13

Align Ornithine aminotransferase; Orn-AT; Lysine aminotransferase; Lys-AT; EC 2.6.1.13; EC 2.6.1.36 (characterized)
to candidate PfGW456L13_2301 Pyoverdin biosynthesis protein PvdH, L-2,4-diaminobutyrate:2-oxoglutarate aminotransferase (EC 2.6.1.76)

Query= SwissProt::Q5JEW1
         (445 letters)



>lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_2301 Pyoverdin
           biosynthesis protein PvdH,
           L-2,4-diaminobutyrate:2-oxoglutarate aminotransferase
           (EC 2.6.1.76)
          Length = 466

 Score =  221 bits (564), Expect = 3e-62
 Identities = 142/425 (33%), Positives = 222/425 (52%), Gaps = 18/425 (4%)

Query: 33  PENLPIVIERGEGIRVYDVDGNVFYDFASGVGVINVGHSHPRVVEAIKKQAEKFTHYSLT 92
           P  +P+ ++R +GI V DV+G  F D  +G G + +GH+HP V+EAI++           
Sbjct: 42  PRRIPLALKRAKGIYVEDVEGRTFIDCLAGAGTLALGHNHPVVIEAIQQVLADELPLHTL 101

Query: 93  DFFYENAIILAEKLIELAPGDI--ERKVVY-GNSGAEANEAAMKLVKYGTGRKQFLAFYH 149
           D          + L  L P  +  E K+ + G +G +A EAA+KLV+  TGR   ++F  
Sbjct: 102 DLTTPVKDRFVQDLFGLLPPALAAEAKIQFCGPTGTDAVEAALKLVRTATGRSTVISFQG 161

Query: 150 AFHGRTQAVLSLTASKWVQQDGFFPTMPGVTHIPYPNPYRNTWGIDGYEEPDELTNRVLD 209
            +HG +Q  LSL  S   ++        GV  +PYP  YR  +G+ G +         L 
Sbjct: 162 GYHGMSQGALSLMGSLGPKKPLGALLGSGVQFMPYPYDYRCPFGLGGAQG----VKANLS 217

Query: 210 FIEEYVFRHVPPHEI-GAIFFEPIQGEGGYVVPPKGFFKALKKFADEYGILLADDEVQMG 268
           ++E  +       ++  A+  E +QGEGG +     + + +++  ++ G+ L  DE+Q G
Sbjct: 218 YLENLLNDPEAGVQLPAAVIVEVVQGEGGVIPADLDWLRGVRRITEQAGVALIVDEIQSG 277

Query: 269 IGRTGKFWAIEHFGVEPDLIQFGKAIGGGLPLAGVIHRADITFDKPGRHATTFGGNPVAI 328
             RTGK +A EH G+ PD++   KAIGG LPLA V++R  +    PG HA TF GN +A+
Sbjct: 278 FARTGKMFAFEHAGIIPDVVVMSKAIGGSLPLAVVVYRDWLDTWLPGAHAGTFRGNQMAM 337

Query: 329 AAGIEVVEIVKE--LLPHVQEVGDYLHKYLEEFKEKYEVIGDARGLGLAQAVEIV----- 381
           AAG  V+  + E  +  H   +G+ L ++L   +  +  +GD RG GL   VE+V     
Sbjct: 338 AAGCAVMRYLVEHKVCEHAAAMGERLAEHLRILQRDFPQLGDIRGRGLMLGVELVDPTGA 397

Query: 382 -KSKETKEKYPELRDRIVKESAKRGLVLLGCGDNS--IRFIPPLIVTKEEIDVAMEIFEE 438
             ++     +  L   + +E  KRGL+L   G +   +RF+PPL++T  +ID   EIF  
Sbjct: 398 LDAQGHPPAFARLAPLVQRECLKRGLILELGGRHGAVVRFLPPLVITAAQIDRVAEIFGR 457

Query: 439 ALKAA 443
           AL AA
Sbjct: 458 ALAAA 462


Lambda     K      H
   0.320    0.141    0.418 

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: 517
Number of extensions: 30
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: 445
Length of database: 466
Length adjustment: 33
Effective length of query: 412
Effective length of database: 433
Effective search space:   178396
Effective search space used:   178396
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 (21.7 bits)
S2: 51 (24.3 bits)

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

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Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
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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