GapMind for Amino acid biosynthesis

 

Alignments for a candidate for agx1 in Sinorhizobium meliloti 1021

Align alanine-glyoxylate transaminase (EC 2.6.1.44) (characterized)
to candidate SMc00294 SMc00294 aminotransferase

Query= BRENDA::D2Z0I0
         (402 letters)



>FitnessBrowser__Smeli:SMc00294
          Length = 405

 Score =  400 bits (1029), Expect = e-116
 Identities = 200/389 (51%), Positives = 264/389 (67%), Gaps = 5/389 (1%)

Query: 7   FPKVKKLPKYVFAMVNELKYQLRREGEDIVDLGMGNPDIPPSQHIIDKLCEVANRPNVHG 66
           F KV++LP YVF  VN LK   R  G DI+DLGMGNPD+P  Q I+DKLCEV   P  H 
Sbjct: 4   FHKVRRLPPYVFEQVNRLKASARAAGADIIDLGMGNPDLPTPQSIVDKLCEVVQDPRTHR 63

Query: 67  YSASKGIPRLRKAICDFYKRRYGVELDPERNAIMTIGAKEGYSHLMLAMLEPGDTVIVPN 126
           YS+SKGIP LR+A   +Y RR+GV+L+PE   + T+G+KEG++++  A+  PGD V+ PN
Sbjct: 64  YSSSKGIPGLRRAQAAYYARRFGVKLNPETQVVATLGSKEGFANMAQAITAPGDVVLCPN 123

Query: 127 PTYPIHYYAPIICGGDAISVPILPEEDFPEVFLRRLYDLIKTSFRKPKAVVLSFPHNPTT 186
           PTYPIH +  ++ GG   S+ + P+E F       L   ++ S  KP A++L++P NPT 
Sbjct: 124 PTYPIHAFGFLMAGGVIRSISVEPDESF----FPPLERAVRHSIPKPLALILNYPSNPTA 179

Query: 187 LCVDLEFFQEVVKLAKQEGIWIVHDFAYADLGFDGYTPPSILQVEGALDVAVELYSMSKG 246
               L+F+++V+  AK+  I ++ D AY+++ FD   PPS+L+V GA DV VE  SMSK 
Sbjct: 180 QVATLDFYKDVIAFAKKHDIIVLSDLAYSEIYFDDAPPPSVLEVPGATDVTVEFTSMSKT 239

Query: 247 FSMAGWRVAFVVGNEMLIKNLAHLKSYLDYGVFTPIQVASIIALESPYEVVEKNREIYRR 306
           FSM GWR+ F VGNE LI  L  +KSYLDYG FTPIQVA+  AL      + + R IY+R
Sbjct: 240 FSMPGWRMGFAVGNERLIAALTRVKSYLDYGAFTPIQVAATQALNGDGSDIAEVRAIYKR 299

Query: 307 RRDVLVEGLNRVGWEVKKPKGSMFVWAKVPEEV-GMNSLDFSLFLLREAKVAVSPGIGFG 365
           RRDV+VE   + G+EV  P  +MF WAK+PE+   + SL+FS  L+ +A VAV+PGIGFG
Sbjct: 300 RRDVMVESFGKAGFEVPPPPATMFAWAKIPEKFRHLGSLEFSKLLVEKADVAVAPGIGFG 359

Query: 366 EYGEGYVRFALVENEHRIRQAVRGIKKAL 394
           E G+ YVR ALVENEHRIRQA R IK+ L
Sbjct: 360 EQGDDYVRLALVENEHRIRQAARNIKRFL 388


Lambda     K      H
   0.322    0.141    0.425 

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: 492
Number of extensions: 16
Number of successful extensions: 3
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: 402
Length of database: 405
Length adjustment: 31
Effective length of query: 371
Effective length of database: 374
Effective search space:   138754
Effective search space used:   138754
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 Apr 09 2024. The underlying query database was built on Apr 09 2024.

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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