GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ptransferase in Klebsiella michiganensis M5al

Align aspartate-prephenate aminotransferase (EC 2.6.1.78) (characterized)
to candidate BWI76_RS07920 BWI76_RS07920 methionine aminotransferase

Query= BRENDA::Q56232
         (385 letters)



>FitnessBrowser__Koxy:BWI76_RS07920
          Length = 386

 Score =  169 bits (429), Expect = 9e-47
 Identities = 113/376 (30%), Positives = 186/376 (49%), Gaps = 17/376 (4%)

Query: 16  TVAVNAKALELRRQGVDLVALTAGEPDFDTPEHVKEAARRALAQGKTKYAPPAGIPELRE 75
           T+     AL  + Q ++L   + G PDFD P +++E     +AQG  +YAP  G+  LRE
Sbjct: 18  TIFSQMSALAQQHQAINL---SQGFPDFDGPRYLQERLAYHVAQGANQYAPMTGVAALRE 74

Query: 76  ALAEKFRRENGLSVTPEETI-VTVGGKQALFNLFQAILDPGDEVIVLSPYWVSYPEMVRF 134
           A+ +K     G        + VT G  +AL+    A++  GDEVI   P + SY   +  
Sbjct: 75  AIVDKTEELYGYRPDANSDVTVTAGATEALYAAITALVRAGDEVICFDPSYDSYAPAIEL 134

Query: 135 AGGVVVEVETLPEEGFVPDPERVRRAITPRTKALVVNSPNNPTGAVYPKEVLEALARLAV 194
           +GGV+  +   P   F  D ++   +++ +T+ +++N+P+NP+  V+ +E   AL +   
Sbjct: 135 SGGVLKRIALQPPH-FRVDWQQFAASLSDKTRLVILNTPHNPSATVWLREDFAALWQAIA 193

Query: 195 EHDFYLVSDEIYEHLLYEGEHFSPGRVAP---EHTLTVNGAAKAFAMTGWRIGYACGPKE 251
           + + Y++SDE+YEH+ +  E  +     P   E  + V+   K F MTGW++GY   P  
Sbjct: 194 DREIYVLSDEVYEHICFAAEGHASVLAHPQLRERAVAVSSFGKTFHMTGWKVGYCVAPAA 253

Query: 252 VIKAMASVSSQSTTSPDTIAQWATLEALTNQEASRAFVEMAREAYRRRRDLLLEGLTALG 311
           +   +  V    T + +T AQ A  + L  +             YR RRDL ++ L +  
Sbjct: 254 ISGELRKVHQYLTFAVNTPAQLAIADMLRREP---EHYRQLPAFYRERRDLFIDALRSSR 310

Query: 312 LKAVRPSGAFYVLMDTSPIAP-DEVRAAERL-LEAGVAVVPGTDFAA--FGH--VRLSYA 365
           L+ +   G +++L D S ++  D+V     L  E GVA +P + F A  F H  +RL +A
Sbjct: 311 LEILPCEGTYFLLADYSAVSDLDDVSFCRWLTTEIGVAAIPLSVFCADPFPHKLIRLCFA 370

Query: 366 TSEENLRKALERFARV 381
                L  A ER  R+
Sbjct: 371 KQPATLLAAAERLCRL 386


Lambda     K      H
   0.317    0.133    0.379 

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: 339
Number of extensions: 19
Number of successful extensions: 5
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: 385
Length of database: 386
Length adjustment: 30
Effective length of query: 355
Effective length of database: 356
Effective search space:   126380
Effective search space used:   126380
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 (21.7 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