GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruH in Sinorhizobium meliloti 1021

Align arginine-pyruvate transaminase (EC 2.6.1.84) (characterized)
to candidate SMc04386 SMc04386 aspartate aminotransferase B protein

Query= BRENDA::Q9HUI9
         (393 letters)



>FitnessBrowser__Smeli:SMc04386
          Length = 410

 Score =  221 bits (562), Expect = 4e-62
 Identities = 132/380 (34%), Positives = 207/380 (54%), Gaps = 15/380 (3%)

Query: 23  RALARVEQGEEILLLSVGDPDFDTPAPIVQAAIDSLLAGNTHYADVRGKRALRQRIAERH 82
           RA A   +G+ +++L  G+PDFDTP  + QAA D++  G T Y  + G   L++ I E+ 
Sbjct: 32  RAAAMKREGKPVIILGAGEPDFDTPEHVKQAASDAIHRGETKYTALDGTPELKKAIREKF 91

Query: 83  RRRSGQAVDAEQVVVLAGAQCALYAVVQCLLNPGDEVIVAEPMYVTYEAVFGACGARVVP 142
           +R +G A + +++ V  GA+  L+  +   L+PGDEVI+  P + +Y  +   C  + V 
Sbjct: 92  QRENGLAYELDEITVATGAKQILFNAMMASLDPGDEVIIPTPYWTSYSDIVHICEGKPVL 151

Query: 143 VPVRSENGFRVQAEEVAALITPRTRAMALNSPHNPSGASLPRATWEALAELCMAH-DLWM 201
           +   + +GFR+ AE++ A ITPRTR + LNSP NPSGA+   A +  L E+ + H  +W+
Sbjct: 152 IACDASSGFRLTAEKLEAAITPRTRWVLLNSPSNPSGAAYSAADYRPLLEVLLRHPHVWL 211

Query: 202 ISDEVYSELLFDG-EHVSPASL-PGMADRTATLNSLSKSHAMTGWRVGWVVGPAALCAHL 259
           + D++Y  +++DG   V+PA L PG+ +RT T+N +SK++AMTGWR+G+  GP  L   +
Sbjct: 212 LVDDMYEHIVYDGFRFVTPAQLEPGLKNRTLTVNGVSKAYAMTGWRIGYAGGPRELIKAM 271

Query: 260 ENLALCMLYGSPEFIQDAACTALEAPLPELEAMREAYRRRRDLVIECLADSPGLRPLRPD 319
             +            Q A+  AL  P   L+   E+++RRRDLV+  L    GL    P+
Sbjct: 272 AVVQSQATSCPSSISQAASVAALNGPQDFLKERTESFQRRRDLVVNGLNAIDGLDCRVPE 331

Query: 320 GGMF-------VMVDIRPTGLSAQA---FADRLLDRHGVSVLAGEAFGPSAAGHIRLGLV 369
           G  +       V+  + P+G   +    F   LL+   V+V+ G AFG S     R+   
Sbjct: 332 GAFYTFSGCAGVLGKVTPSGKRIKTDTDFCAYLLEDAHVAVVPGSAFGLSP--FFRISYA 389

Query: 370 LGAEPLREACRRIALCAAEL 389
                L+EA  RIA     L
Sbjct: 390 TSEAELKEALERIAAACDRL 409


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: 423
Number of extensions: 25
Number of successful extensions: 4
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: 410
Length adjustment: 31
Effective length of query: 362
Effective length of database: 379
Effective search space:   137198
Effective search space used:   137198
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