GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruH in Pseudomonas simiae WCS417

Align arginine-pyruvate transaminase (EC 2.6.1.84) (characterized)
to candidate GFF2657 PS417_13545 arginine aminotransferase

Query= BRENDA::Q9HUI9
         (393 letters)



>FitnessBrowser__WCS417:GFF2657
          Length = 664

 Score =  398 bits (1022), Expect = e-115
 Identities = 202/392 (51%), Positives = 265/392 (67%)

Query: 1   MRYSDFTQRIAGDGAAAWDIHYRALARVEQGEEILLLSVGDPDFDTPAPIVQAAIDSLLA 60
           MR+S F +RIAG G AAWDIH+ A     QGE+I++LSVGDPDF TP+ I  AA+ +L  
Sbjct: 1   MRFSPFVERIAGQGVAAWDIHHAAFQAASQGEDIIILSVGDPDFATPSFITDAAVSALRE 60

Query: 61  GNTHYADVRGKRALRQRIAERHRRRSGQAVDAEQVVVLAGAQCALYAVVQCLLNPGDEVI 120
           G+THY ++ G+ ALR+ IA R+ +   +A+ AE V+ +AGAQ AL+    CLL  GDEV+
Sbjct: 61  GDTHYTEIPGRPALREAIAARYSKTLARALSAENVITVAGAQNALFVTSLCLLQAGDEVL 120

Query: 121 VAEPMYVTYEAVFGACGARVVPVPVRSENGFRVQAEEVAALITPRTRAMALNSPHNPSGA 180
           V +PMYVTYEA   A GA +V VP   E+GFR+ A+ + A ITPRTRA+  ++P+NP+G 
Sbjct: 121 VLDPMYVTYEATLKASGATLVRVPCSPESGFRLDAQLLGAAITPRTRAIFFSNPNNPTGV 180

Query: 181 SLPRATWEALAELCMAHDLWMISDEVYSELLFDGEHVSPASLPGMADRTATLNSLSKSHA 240
            L     +A+A+L +A DLW++ DEVY  L+FDGE+ S A+LPGMA+R   + SLSKSHA
Sbjct: 181 VLNLQELQAIADLAIARDLWVVVDEVYESLVFDGEYHSLAALPGMAERCVVIGSLSKSHA 240

Query: 241 MTGWRVGWVVGPAALCAHLENLALCMLYGSPEFIQDAACTALEAPLPELEAMREAYRRRR 300
           MTGWR+GW++    + AH E L L MLYG P F+ +AA  A+ A     + MRE YRRRR
Sbjct: 241 MTGWRIGWIIATPQMVAHAETLVLSMLYGLPGFVMEAATAAVLAHDDVTQGMREIYRRRR 300

Query: 301 DLVIECLADSPGLRPLRPDGGMFVMVDIRPTGLSAQAFADRLLDRHGVSVLAGEAFGPSA 360
           DLV+  L+  PG++   P  GMFV+VD+R TGL +  FA RL    GVSVL   AFG  A
Sbjct: 301 DLVMAGLSACPGIKVQAPQAGMFVLVDVRGTGLGSLDFAWRLFREAGVSVLDAAAFGAPA 360

Query: 361 AGHIRLGLVLGAEPLREACRRIALCAAELLGQ 392
            G +RL   LG E L EAC+RIA   A+L G+
Sbjct: 361 QGFVRLSFTLGEERLSEACQRIAHFVAKLAGE 392


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: 710
Number of extensions: 20
Number of successful extensions: 2
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: 664
Length adjustment: 34
Effective length of query: 359
Effective length of database: 630
Effective search space:   226170
Effective search space used:   226170
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: 52 (24.6 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