GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Pseudomonas stutzeri RCH2

Align Probable aspartate/prephenate aminotransferase; AspAT / PAT; EC 2.6.1.1; EC 2.6.1.78; Transaminase A (uncharacterized)
to candidate GFF1734 Psest_1772 Aspartate/tyrosine/aromatic aminotransferase

Query= curated2:O67781
         (394 letters)



>FitnessBrowser__psRCH2:GFF1734
          Length = 403

 Score =  157 bits (396), Expect = 7e-43
 Identities = 115/354 (32%), Positives = 177/354 (50%), Gaps = 17/354 (4%)

Query: 24  AKELRAKGVDVIGFGAGEP---DFDTPDFIKEACIRALREGKTKYAPSAGIPELREAIAE 80
           AK L  +G  ++    G P    F+ P+ I +  IR L   +  Y+ S G+   R+AI +
Sbjct: 24  AKRLEEEGHRILKLNIGNPAPFGFEAPEEILQDVIRNLPTAQG-YSDSKGLFSARKAIMQ 82

Query: 81  KLLKENKVEYKPSEIVVSAGAKMVLFLIFMAILDEGDEVLLPSPYWVTYPEQIRFFGGVP 140
              ++        +I +  G   ++ +   A+L+ GDEVL+P+P +  +   +   GG P
Sbjct: 83  YYQQKQVEGVSIEDIYLGNGVSELIVMSMQALLNNGDEVLIPAPDYPLWTAAVSLAGGKP 142

Query: 141 VEVPLKKEKGFQLSLEDVKEKVTERTKAIVINSPNNPTGAVYEEEELKKIAEFCVERGIF 200
           V     ++  +   L D+K K+T  TKA+V+ +PNNPTGAVY +E L+ + E   +  + 
Sbjct: 143 VHYLCDEQANWWPDLADIKAKITPNTKALVLINPNNPTGAVYPKEVLEGMVELARQHKLV 202

Query: 201 IISDECYEYFVYGDAKFVSPASFSDEVKNITFTVNAFSKSYSMTGWRIGYVAC------P 254
           + SDE Y+  +Y DA  +S AS + +V  +TF  N  SKSY + G+R G+VA        
Sbjct: 203 LFSDEIYDKILYDDAVHISTASLAPDVLCLTF--NGLSKSYRVAGFRSGWVAISGPKHKA 260

Query: 255 EEYAKVIASL-NSQSVSNVTTFAQYGALEALKNPKS-KDFVNEMRNAFERRRDTAVEELS 312
           + Y + +  L N +  +NV   AQ+    AL   +S  D V       E+R  T  E L+
Sbjct: 261 QSYIEGLDILANMRLCANVP--AQHAIQTALGGYQSINDLVLPPGRLLEQRNRT-WELLN 317

Query: 313 KIPGMDVVKPEGAFYIFPDFSAYAEKLGGDVKLSEFLLEKAKVAVVPGSAFGAP 366
            IPG+  VKP GA Y FP        +  D K    LL   K+ +V G+AF  P
Sbjct: 318 DIPGISCVKPMGALYAFPRIDPKICPIHNDEKFVLDLLLSEKLLIVQGTAFNWP 371


Lambda     K      H
   0.317    0.135    0.383 

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: 349
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: 394
Length of database: 403
Length adjustment: 31
Effective length of query: 363
Effective length of database: 372
Effective search space:   135036
Effective search space used:   135036
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 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