GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruH in Pseudomonas putida KT2440

Align arginine-pyruvate transaminase (EC 2.6.1.84) (characterized)
to candidate PP_3721 PP_3721 Arginine--pyruvate transaminase AruH

Query= BRENDA::Q9HUI9
         (393 letters)



>FitnessBrowser__Putida:PP_3721
          Length = 396

 Score =  636 bits (1641), Expect = 0.0
 Identities = 316/390 (81%), Positives = 347/390 (88%)

Query: 1   MRYSDFTQRIAGDGAAAWDIHYRALARVEQGEEILLLSVGDPDFDTPAPIVQAAIDSLLA 60
           MRY+  TQRIAGDGAAAWDIHYRALA   + ++ILLLSVGDPDFDTPAPIV+AAIDSL A
Sbjct: 1   MRYAKLTQRIAGDGAAAWDIHYRALALQAEDKDILLLSVGDPDFDTPAPIVEAAIDSLRA 60

Query: 61  GNTHYADVRGKRALRQRIAERHRRRSGQAVDAEQVVVLAGAQCALYAVVQCLLNPGDEVI 120
           G+THYADVRGK ALRQ IA RHR+RSGQAV A+QV VLAGAQCALY V QC+L+PGDEVI
Sbjct: 61  GHTHYADVRGKLALRQAIANRHRQRSGQAVSADQVTVLAGAQCALYCVAQCILDPGDEVI 120

Query: 121 VAEPMYVTYEAVFGACGARVVPVPVRSENGFRVQAEEVAALITPRTRAMALNSPHNPSGA 180
           VAEPMYVTYEAVFGACGA+VVPVPV+ ENGFRV   +VA  ITPRTRA+ALNSPHNPSGA
Sbjct: 121 VAEPMYVTYEAVFGACGAKVVPVPVKPENGFRVCPRDVAERITPRTRALALNSPHNPSGA 180

Query: 181 SLPRATWEALAELCMAHDLWMISDEVYSELLFDGEHVSPASLPGMADRTATLNSLSKSHA 240
           SLPRATWEALAELC+AHDLW+ISDEVYSELL++GEHVSP SLPGMA+RTATLNSLSKSHA
Sbjct: 181 SLPRATWEALAELCVAHDLWLISDEVYSELLYEGEHVSPGSLPGMAERTATLNSLSKSHA 240

Query: 241 MTGWRVGWVVGPAALCAHLENLALCMLYGSPEFIQDAACTALEAPLPELEAMREAYRRRR 300
           MTGWR+GWVVG  AL  HLENLALCMLYG P+F+QDAA  ALE PLPEL+AMREAYR+RR
Sbjct: 241 MTGWRMGWVVGSTALATHLENLALCMLYGLPDFVQDAAVVALEHPLPELDAMREAYRQRR 300

Query: 301 DLVIECLADSPGLRPLRPDGGMFVMVDIRPTGLSAQAFADRLLDRHGVSVLAGEAFGPSA 360
           DLV E LA  PGL+ L+PDGGMFVM+DIR TG+SAQAFAD LLD  GVSVLAGEAFGPSA
Sbjct: 301 DLVCEQLAGCPGLKALKPDGGMFVMLDIRETGVSAQAFADYLLDSQGVSVLAGEAFGPSA 360

Query: 361 AGHIRLGLVLGAEPLREACRRIALCAAELL 390
           AGHIRLGLVLG E L +AC+RIA CA EL+
Sbjct: 361 AGHIRLGLVLGNEALVDACQRIARCAGELM 390


Lambda     K      H
   0.322    0.136    0.411 

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: 664
Number of extensions: 20
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: 393
Length of database: 396
Length adjustment: 31
Effective length of query: 362
Effective length of database: 365
Effective search space:   132130
Effective search space used:   132130
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 (21.9 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