GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argD in Echinicola vietnamensis KMM 6221, DSM 17526

Align Acetylornithine aminotransferase; ACOAT; EC 2.6.1.11 (uncharacterized)
to candidate Echvi_2919 Echvi_2919 Ornithine/acetylornithine aminotransferase

Query= curated2:Q8TUZ5
         (389 letters)



>FitnessBrowser__Cola:Echvi_2919
          Length = 393

 Score =  276 bits (707), Expect = 6e-79
 Identities = 139/373 (37%), Positives = 237/373 (63%), Gaps = 10/373 (2%)

Query: 20  VTLVPGEGARVWDDEGNEYIDLVAGIAVNVLGHCHPAVVEAVKEQVERLIHCS--NLYYN 77
           + +   EG  ++  +G +YIDL++GI V+ +GH HP V++A+++Q+++ +H      Y  
Sbjct: 21  IEIEKAEGIYMYGPKGEKYIDLISGIGVSNVGHRHPKVLKAIQDQLDKYMHLMVYGEYVQ 80

Query: 78  EPQAEAARLLAEAAPKDLNKVFFCNSGTESVECAIKLARKFTGCTKFIAFEGGFHGRTMG 137
            PQ + A+ L +  PK L+ V+  NSG+E+VE A+KLA+++TG  + ++    +HG + G
Sbjct: 81  SPQTQLAKALTDTLPKKLDNVYLVNSGSEAVEGALKLAKRYTGRREILSCVNAYHGSSHG 140

Query: 138 ALSATWKPEFREPFEPLVPEFEHVPYGDVNAVEKAIDDDTAAVIVEPVQGEAGVRIPPEG 197
           ALS      F+  + PL+P   H+ + + + +++ I ++TAA++VE VQGEAG+R+  + 
Sbjct: 141 ALSVGGNEIFKRAYRPLLPGIRHLDFNEPDQLDQ-ITEETAAIMVETVQGEAGIRVGTKE 199

Query: 198 FLRELRELCDEHGLLLIVDEVQSGMGRTGQFFAFEHEDVLPDIVCLAKGLGGGVPVGATI 257
           + + LR  CDE G LLI+DE+Q+G GRTG+F+AF+H D++PDIV  AKG+GGG+P+GA I
Sbjct: 200 YFKALRHRCDETGTLLILDEIQAGFGRTGKFWAFQHYDIVPDIVVCAKGMGGGMPIGAFI 259

Query: 258 AREEVAEAFEPG---DHGSTFGGNPLACAAVCAAVSTVLEENLPEAAERKGKLAMRILSE 314
           A + +   F+      H +TFGG+P++CAA  A +  + +E L +  ERK  L  + L+ 
Sbjct: 260 APQSIMSVFKNNPLLGHITTFGGHPVSCAAALATIDILRDEKLIQHVERKANLFKKHLNH 319

Query: 315 AEDVVEEVRGRGLMMGVEVGDDERAKDVAREMLDRGALVN--VTSGDVIRLVPPLVIGED 372
            +  ++E+R +GLMM V+    E  K +    ++ G + +  +   D +R+ PPL I ++
Sbjct: 320 PK--IQEIRNKGLMMAVKFEAFEVLKPIIDRAIELGIITDWFLFCEDSMRIAPPLTITDE 377

Query: 373 ELEKALAELADAL 385
           E+EKA A +  ++
Sbjct: 378 EIEKACAIILQSI 390


Lambda     K      H
   0.318    0.137    0.405 

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: 376
Number of extensions: 22
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: 389
Length of database: 393
Length adjustment: 31
Effective length of query: 358
Effective length of database: 362
Effective search space:   129596
Effective search space used:   129596
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