GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PPYAT in Acidithiobacillus ferrooxidans ATCC 23270

Align aspartate transaminase (EC 2.6.1.1) (characterized)
to candidate WP_012536158.1 AFE_RS02230 alanine transaminase

Query= BRENDA::Q8YTF2
         (403 letters)



>NCBI__GCF_000021485.1:WP_012536158.1
          Length = 393

 Score =  358 bits (920), Expect = e-103
 Identities = 183/381 (48%), Positives = 243/381 (63%), Gaps = 3/381 (0%)

Query: 10  DRIQQLPPYVFARLDELKAKAREQGIDLIDLGMGNPDGATPQPVVDAAIQALQDPKNHGY 69
           +RI++LPPYVF  + +LK +AR++G D+ID GMGNPD  TPQ +VD   +  Q    H Y
Sbjct: 6   ERIRRLPPYVFNIVTDLKNQARKRGEDIIDFGMGNPDQPTPQYIVDKLCETAQRGDTHRY 65

Query: 70  PPFEGTASFRRAITNWYNRRYGVVLDPDSEALPLLGSKEGLSHLAIAYVNPGDVVLVPSP 129
               G    RRAIT WY  RYGV LDP+SEA+  +GSKEG++HLA+A + PGD VLVPSP
Sbjct: 66  SVSRGIPRLRRAITTWYEHRYGVQLDPESEAIVTIGSKEGIAHLALATMGPGDTVLVPSP 125

Query: 130 AYPAHFRGPVIAGGTVHSLILKPENDWLIDLTAIPEEVARKAKILYFNYPSNPTGATAPR 189
            YP H  G VIAG  V  + + P  D+  +L         K K+L  N+P NPT A    
Sbjct: 126 TYPIHPYGFVIAGADVRHVPMLPGVDFFEELEKAVRAAWPKPKMLVINFPHNPTAAVVDL 185

Query: 190 EFFEEIVAFARKYEILLVHDLCYAELAFDGYQPTSLLEIPGAKDIGVEFHTLSKTYNMAG 249
           +FF  IVAFA+++ I +VHDL YA++ FDGY   S L++PGAKD+GVEF TLSK+YNM G
Sbjct: 186 DFFARIVAFAKEHRIWVVHDLAYADIVFDGYTAPSFLQVPGAKDVGVEFFTLSKSYNMPG 245

Query: 250 WRVGFVVGNRHVIQGLRTLKTNLDYGIFAALQTAAETALQLPDIYLHEVQQRYRTRRDFL 309
           WRVGF VGN  ++  L  +K+ LDYG F  +Q AA TAL+ P   + +++  Y  RRD L
Sbjct: 246 WRVGFAVGNPKLVGALARMKSYLDYGTFTPIQVAAITALEGPQDCVEDIRLMYEQRRDVL 305

Query: 310 IQGLGELGWDVPKTKATMYLWVKCPVG---MGSTDFALNLLQQTGVVVTPGNAFGVAGEG 366
            +GL   GW V K KATM++W + P     MGS +F+  +L++  V V+PG  FG  G+ 
Sbjct: 306 CEGLDAAGWAVDKPKATMFVWARIPESLRRMGSLEFSKLVLERARVAVSPGIGFGDLGDE 365

Query: 367 YVRISLIADCDRLGEALDRIK 387
           YVR  L+ +  R  +A+  IK
Sbjct: 366 YVRFGLVENEHRTRQAIRGIK 386


Lambda     K      H
   0.321    0.140    0.427 

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: 494
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: 403
Length of database: 393
Length adjustment: 31
Effective length of query: 372
Effective length of database: 362
Effective search space:   134664
Effective search space used:   134664
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 (21.8 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