GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvE in Dyella japonica UNC79MFTsu3.2

Align branched-chain-amino-acid transaminase (EC 2.6.1.42) (characterized)
to candidate N515DRAFT_3366 N515DRAFT_3366 GntR family transcriptional regulator / MocR family aminotransferase

Query= BRENDA::A0A060PQX5
         (417 letters)



>FitnessBrowser__Dyella79:N515DRAFT_3366
          Length = 480

 Score =  176 bits (446), Expect = 1e-48
 Identities = 111/362 (30%), Positives = 181/362 (50%), Gaps = 16/362 (4%)

Query: 52  GLPAPETFPVEIIAEITKEVLEKHAAQALQYGTTKGFTPLRLALAEWMRKRYDIPISKVD 111
           G+P    FP E+   ++   L   +      G ++G   LR A+A+ +     +     D
Sbjct: 131 GVPDTRQFPFEVWRRLSARALRDVSRLPSMSGQSRGRPILREAIAQHVSFARAVACDPDD 190

Query: 112 IMITSGSQQALDLIGRVFINPGDIVV-VEAPTYLAALQAFKYYEPEFVQIPLDDEGMRVD 170
           +M+TSG+QQA DL+ RV + PG  VV +E P Y     AF       V + +DDEG+ V 
Sbjct: 191 VMVTSGAQQAFDLLARVLVTPGKTVVAMEDPGYTPLRAAFAAAGARLVPVAVDDEGIVV- 249

Query: 171 LLEEKLQELEKEGKKVKLVYTIPTFQNPAGVTMSEKRRKRLLELASEYDFLIVEDNPYGE 230
                    E+   + +++Y  P+ Q P G++MS +RR  LL  A+     ++ED+  GE
Sbjct: 250 ---------ERIPVEARVIYVTPSHQFPLGMSMSPRRRAELLAFAAARRATVIEDDYDGE 300

Query: 231 LRYSGEPVKPIKAWDDEGRVMYLGTFSKILAPGFRIGWIAAEPHLIRKLEIAKQSVDL-C 289
            RY G P+  ++  D EG V Y+GTFSK L P  RIG++ A P L+  L  AK+  D  C
Sbjct: 301 FRYGGRPLDALQTLDREGSVCYVGTFSKCLFPALRIGYLVAPPWLLPALAAAKELADWHC 360

Query: 290 TNPFSQVIAWKYVEGGHLDNHIPNIIEFYKPRRDAMLKALEEFMPEGVRWTKPEGGMFVW 349
             P    +A  ++  GHL  H+  + + Y  RR+A+L AL      G+     + G+ + 
Sbjct: 361 DVPAQDTLA-AFIAEGHLARHVRRMRKIYAERREALLDALAR---HGLEAWPSDAGLHLS 416

Query: 350 VTLPEGIDTKLMLEKAVAKGVAYVPGEAFFAHRDVKNTMRLNFTYVPEEKIREGIKRLAE 409
             LP  + T +++E+A A+GV     + +   R   N + L +  +   ++ E ++ +A 
Sbjct: 417 AKLPRKLRTDVLVEQAAARGVRIEGLDGYTFGRASANGLALGYGLIEAARMDEAVRHIAR 476

Query: 410 TI 411
            +
Sbjct: 477 LL 478


Lambda     K      H
   0.318    0.137    0.398 

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: 429
Number of extensions: 18
Number of successful extensions: 4
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: 417
Length of database: 480
Length adjustment: 33
Effective length of query: 384
Effective length of database: 447
Effective search space:   171648
Effective search space used:   171648
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: 51 (24.3 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