GapMind for Amino acid biosynthesis

 

Alignments for a candidate for agx1 in Klebsiella michiganensis M5al

Align 3-hydroxykynurenine transaminase; AgHKT; Alanine--glyoxylate aminotransferase; EC 2.6.1.63; EC 2.6.1.44 (characterized)
to candidate BWI76_RS10590 BWI76_RS10590 class V aminotransferase

Query= SwissProt::Q7PRG3
         (396 letters)



>FitnessBrowser__Koxy:BWI76_RS10590
          Length = 413

 Score =  232 bits (591), Expect = 2e-65
 Identities = 130/362 (35%), Positives = 203/362 (56%), Gaps = 22/362 (6%)

Query: 17  PEKIMMGPGPSNCSKRVLTAMTNTVLSNFHAELFRTMDEVKDGLRYIFQTENRATMCVSG 76
           P +++MGPGP N   RVL AM++ ++  +   +   M+EV    R +F+TENR TM V G
Sbjct: 12  PSRLLMGPGPINADPRVLRAMSSQLIGQYDPAMTHYMNEVMALYRGVFRTENRWTMLVDG 71

Query: 77  SAHAGMEAMLSNLLEEGDRVLIAVNGIWAERAVEMSERYGADVRTIEGPPDRPFSLETLA 136
           ++ AG+EA+L + +  GD+VL+ V G +     E++ R  A+V TIE P    F+ + + 
Sbjct: 72  TSRAGIEAILVSAIRPGDKVLVPVFGRFGHLLCEIARRCRAEVHTIEVPWGEVFTPDQVE 131

Query: 137 RAIELHQPKCLFLTHGDSSSGLLQPLEGVGQICHQHDCLLIVDAVASLCGVPFYMDKWEI 196
            A++  +P+ L    GD+S+ +LQPL  +G+IC ++D L   DA ASL G P   D W +
Sbjct: 132 DAVKRIRPRLLLTVQGDTSTTMLQPLAELGEICRRYDALFYTDATASLGGNPLETDVWGL 191

Query: 197 DAVYTGAQKVLGAPPGITPISISPKALDVIRNRRTKSKVF----------------YWDL 240
           DAV  G QK LG P G +PI++S +  + IR R+   +                  Y+DL
Sbjct: 192 DAVSAGMQKCLGGPSGTSPITLSARMEEAIRRRKCVEEGIRTDAHRDGDEEMIYSNYFDL 251

Query: 241 LLLGNYWGCYDEPKRY-HHTVASNLIFALREALAQIAEEGLENQIKRRIECAQILYEGLG 299
            ++ +YWG    P+R  HHT A+  +F  RE    I +EGL+  I R       L +G+ 
Sbjct: 252 GMVMDYWG----PERLNHHTEATTALFGARECARLILQEGLDYGIARHKLHGDALVKGIQ 307

Query: 300 KMGLDIFVKDPRHRLPTVTGIMIPKGVDWWKVSQYAMNNFSLEVQGGLGPTFGKAWRVGI 359
            MGL+ F  D +H++  V G++IP+G++  +  +  + +F +E+    GP  GK WR+G 
Sbjct: 308 AMGLETF-GDLKHKMNNVLGVVIPQGINGDQARKLMLEDFGIEIGTSFGPLHGKVWRIGT 366

Query: 360 MG 361
           MG
Sbjct: 367 MG 368


Lambda     K      H
   0.321    0.138    0.430 

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: 437
Number of extensions: 21
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: 396
Length of database: 413
Length adjustment: 31
Effective length of query: 365
Effective length of database: 382
Effective search space:   139430
Effective search space used:   139430
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