GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Heliobacterium modesticaldum Ice1; ATCC 51547

Align branched-chain-amino-acid transaminase (EC 2.6.1.42); glutamate-prephenate aminotransferase (EC 2.6.1.79) (characterized)
to candidate WP_083765180.1 HM1_RS06865 branched-chain-amino-acid transaminase

Query= BRENDA::P54691
         (305 letters)



>NCBI__GCF_000019165.1:WP_083765180.1
          Length = 362

 Score =  128 bits (321), Expect = 2e-34
 Identities = 94/279 (33%), Positives = 147/279 (52%), Gaps = 25/279 (8%)

Query: 7   IAYFEDKFVPFEDAKISVATHALHYGTAAFGGLRGIPDPEDPGTILLFRLDRHGDRLSKS 66
           I Y +  FVP E A+ISV  H   YG   F G+R            +F+LD H DRL  S
Sbjct: 76  IIYLDGCFVPEEQARISVFDHGFLYGDGIFEGIRAYNGR-------VFKLDAHIDRLYDS 128

Query: 67  AKFLHYDISAEK--IKEVIVDFVKKNQPDKSFYIRPLVYSSG---LGIAPR------LHN 115
           AK +   I   K  + +V+++ +++N   +  YIR LV S G   LG+ PR      +  
Sbjct: 129 AKAIQLAIPMGKGEMVDVVLETLRRNHL-RDAYIR-LVVSRGKGDLGLDPRKCPGATVMC 186

Query: 116 LEKDFLVYGLEMGDYLAADGVSCRISSWYRQEDRSFPLRGKISAAYITSALAKTEAVESG 175
           +     +Y  E  +     G+     +  R    +   R K S  Y+ + LAK EA ++G
Sbjct: 187 IAAGITLYPPEFYE----KGLEVVTVATRRNVPEALNPRIK-SLNYLNNILAKLEAAKAG 241

Query: 176 FDEAILMNSQGKVCEATGMNVFMVRNGQIVTPGNEQDILEGITRDSILTIAADLGIPTCQ 235
             EAI++N +G V E TG N+F+++  +++TP     ILEGITR++++ +A + GIP  +
Sbjct: 242 VLEAIMLNQEGYVAECTGDNIFIIKQRRLITPPVHVGILEGITRNTVMDLAREKGIPVVE 301

Query: 236 RPIDKSELMIADEVFLSGTAAKITPVKRIENFTLGGDRP 274
               + ++  ADEVFL+GTAA++ PV  ++  T+G   P
Sbjct: 302 AVFTRFDVYTADEVFLTGTAAEVIPVVTVDGRTIGEGVP 340


Lambda     K      H
   0.320    0.138    0.406 

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: 247
Number of extensions: 10
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 305
Length of database: 362
Length adjustment: 28
Effective length of query: 277
Effective length of database: 334
Effective search space:    92518
Effective search space used:    92518
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: 49 (23.5 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.

Links

Downloads

Related tools

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