GapMind for Amino acid biosynthesis

 

Alignments for a candidate for ilvE in Desulfovibrio vulgaris Hildenborough

Align branched-chain-amino-acid transaminase (EC 2.6.1.42) (characterized)
to candidate 207560 DVU2086 transcriptional regulator, GntR family

Query= BRENDA::A0A060PQX5
         (417 letters)



>MicrobesOnline__882:207560
          Length = 480

 Score =  150 bits (379), Expect = 8e-41
 Identities = 112/372 (30%), Positives = 178/372 (47%), Gaps = 10/372 (2%)

Query: 44  SDVISLAGGLPAPETFPVEIIAEITKEVLEKHAAQALQYGTTKGFTPLRLALAEWMRKRY 103
           S V+S   G+PA + FP E  A   + V       AL+Y    G   LR A+A ++R+  
Sbjct: 106 SGVVSFRSGIPALDVFPREEWARTYQRVCAALPDDALRYSAPAGVWALREAIAGYLRRTR 165

Query: 104 DIPISKVDIMITSGSQQALDLIGRVFINPGDIVVVEAPTYLAALQAFKYYEPEFVQIPLD 163
            I      +MITSG+ Q L ++ R+    G +V+ E P +    +  +        +P+D
Sbjct: 166 GIRCHAERVMITSGATQGLRIMSRLLQRSGGVVLAEDPAHAGLREVLEVTGLRVEGVPVD 225

Query: 164 DEGMRVDLLEEKLQELEKEGKKVKLVYTIPTFQNPAGVTMSEKRRKRLLELASEYDFLIV 223
           D GM   +L    +E  + G  V  VY  P+ Q P G  +  +RR+ L+  A E + LIV
Sbjct: 226 DRGMDTGML-PSAEEARRAG--VAFVYVTPSHQYPLGGILPVQRRQALVRFAREAECLIV 282

Query: 224 EDNPYGELRYSGEPVKPIKAWDDEGRVMYLGTFSKILAPGFRIGWIAAEPHLIRKLEIAK 283
           ED+  GE R+ G PV  +     E  V+YLG+FSK+LAP  R+G+      L+      K
Sbjct: 283 EDDYDGEFRHEGSPVGTLHELAPES-VVYLGSFSKVLAPALRLGFAILPARLLAAWHREK 341

Query: 284 QSVDLCTNPFSQVIAWKYVEGGHLDNHIPNIIEFYKPRRDAMLKALEEFMPEGVRWTKPE 343
              D+ T+  SQ     ++  G L+ HI  + + Y+ RR  ++K+L     + V      
Sbjct: 342 LYSDVHTDALSQHALASFIGSGALERHIWRMKKLYRRRRAFLVKSLMRHFGDAVGIRGHA 401

Query: 344 GGMFVWVTLPEGI--DTKLMLEKAVAKGVAYVPGEAFFAHR--DVKNTMRLNFTYVPEEK 399
            G+ + V    G+  D K+M E A   GV   P  A+      D  N + L + ++ EE 
Sbjct: 402 TGLHL-VAAFTGVRFDDKVMSELA-RGGVEATPVHAYALQHGDDHVNELILGYAHLSEEA 459

Query: 400 IREGIKRLAETI 411
           + +G++ L + +
Sbjct: 460 MEQGVRLLKQVL 471


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: 453
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: 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