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 SMc02262 SMc02262 aminotransferase

Query= BRENDA::Q9HUI9
         (393 letters)



>FitnessBrowser__Smeli:SMc02262
          Length = 396

 Score =  300 bits (767), Expect = 6e-86
 Identities = 156/386 (40%), Positives = 227/386 (58%), Gaps = 1/386 (0%)

Query: 1   MRYSDFTQRIAGDGAAAWDIHYRALARVEQGEEILLLSVGDPDFDTPAPIVQAAIDSLLA 60
           MRY+  T R+A  G+  W +H RA      G E++ L++G+PD      +++    ++ A
Sbjct: 1   MRYASITSRLAELGSGKWTLHTRARQLKASGAELIELTIGEPDLPPDRALLEECQRAMNA 60

Query: 61  GNTHYADVRGKRALRQRIAERHRRRSGQAVDAEQVVVLAGAQCALYAVVQCLLNPGDEVI 120
           G   Y++ RG+ A+   + E++RRR   AV AE ++   G Q AL+AV+  L   GD V+
Sbjct: 61  GRYRYSNGRGEPAVVAALTEKYRRRRA-AVTAENILCFPGTQTALFAVMFALAEAGDGVL 119

Query: 121 VAEPMYVTYEAVFGACGARVVPVPVRSENGFRVQAEEVAALITPRTRAMALNSPHNPSGA 180
           V +P+Y TYE V  + GA  V VP+  ENGF ++AE++   +TP  R + LN+PHNP+GA
Sbjct: 120 VGDPLYATYEGVIRSTGAHPVFVPLNPENGFHMRAEDLEKAVTPECRVLLLNTPHNPTGA 179

Query: 181 SLPRATWEALAELCMAHDLWMISDEVYSELLFDGEHVSPASLPGMADRTATLNSLSKSHA 240
            L      A+ E+   HDLW++ DEVY EL+FD    SP   P +A+RT  ++S+SKSHA
Sbjct: 180 VLTAEEIAAIGEVARRHDLWIVCDEVYEELVFDALFASPFDNPDLAERTVVVSSISKSHA 239

Query: 241 MTGWRVGWVVGPAALCAHLENLALCMLYGSPEFIQDAACTALEAPLPELEAMREAYRRRR 300
             G+R GW VGPA     L  ++  ML+G   FI D    AL   +     MRE+Y RR 
Sbjct: 240 APGFRSGWAVGPAEFTERLLPISETMLFGQQPFIADMTAYALTHDIDTARQMRESYSRRA 299

Query: 301 DLVIECLADSPGLRPLRPDGGMFVMVDIRPTGLSAQAFADRLLDRHGVSVLAGEAFGPSA 360
             +I+ LA + G+  L P+ GMF ++D+  TGLS +AFA  LL+  GV+V+ G +FG  A
Sbjct: 300 RRIIDGLAGASGVSVLPPEAGMFALIDVSGTGLSGEAFAWALLEEEGVAVMPGSSFGDKA 359

Query: 361 AGHIRLGLVLGAEPLREACRRIALCA 386
              +R+ L +    + EACRRIA  A
Sbjct: 360 RNFLRVSLTVPDAAIEEACRRIAALA 385


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: 469
Number of extensions: 23
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: 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