GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gatD in Pseudomonas stutzeri RCH2

Align Glutamyl-tRNA(Gln) amidotransferase subunit D; Glu-ADT subunit D; EC 6.3.5.- (uncharacterized)
to candidate GFF4005 Psest_4078 L-asparaginase/archaeal Glu-tRNAGln amidotransferase subunit D

Query= curated2:Q9Y9T8
         (427 letters)



>FitnessBrowser__psRCH2:GFF4005
          Length = 327

 Score =  105 bits (262), Expect = 2e-27
 Identities = 100/348 (28%), Positives = 157/348 (45%), Gaps = 35/348 (10%)

Query: 74  ERVYIIGAGGTIASRVD----YETGAVKPYLDASELATTIPELQRYASIEAEQLFSILSE 129
           ER+ ++  GGTI  +            +  L A +   T P L  +   E + L    S 
Sbjct: 6   ERLLVLYTGGTIGMQQSAAGLMPASGFEARLRAQQALETGP-LPSWTFRELQPLLD--SA 62

Query: 130 DMKPSMWEAIVDRAAR-VLEAGYDGVVVAHGTDTMAFTASALSFAFHKGLPSPVILTGSQ 188
           +M+PS W  +       V ++  D V++ HGTDT+A++A+ALSF     L  PV+LTG+ 
Sbjct: 63  NMQPSHWLQMATAVREAVAQSDCDAVLLLHGTDTLAYSAAALSFLL-LDLEIPVLLTGAM 121

Query: 189 RSSDRPSSDAAFNLTASVLAASRAPFAEVAVVMHGETGDTYALAHRGVRVKKMHSSRRDA 248
             +  P SDA  NL  ++ A        V +  +G       L H G RV K+ S   DA
Sbjct: 122 LPAGSPGSDAWPNLFGAMRALQAGRVEGVRLFFNG------VLLH-GARVSKLRSDAFDA 174

Query: 249 FQSVNDKPLARIYPFEGRVEMLRDDYRRRGESGLEVDNGFEERVALVKHFPGLISEVIDA 308
           F     K  A +                 GE    +      +V ++  +PG+ +  + A
Sbjct: 175 FAEAPRKRSATVV----------------GERPPMLLPQQPAQVVVLPLYPGVGAAQVQA 218

Query: 309 LLDRGFKGIVVE--GTGFGHVS-SDAIKSIERARDQGVPIVITTQTVFGRVNLNVYSTGR 365
           L+  G + +++E  G+G G    +  I+++ +A  QGV +   +Q   G V+  VY+TG 
Sbjct: 219 LVASGAQALLLECYGSGTGPAGDAPFIEALRQAHRQGVVLAAISQCPGGHVDFGVYATGS 278

Query: 366 KMLAAGAIPAGDMTSEAAYAKLSWILARTRELEVVRKMFQRNLAGEVS 413
            +  AG +  G MT EAA  KL  +L        V   F R+L GE++
Sbjct: 279 GLRDAGLVSGGGMTREAALGKLFALLTAGLNQAQVEHWFCRDLCGEMA 326


Lambda     K      H
   0.318    0.136    0.385 

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: 322
Number of extensions: 20
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: 427
Length of database: 327
Length adjustment: 30
Effective length of query: 397
Effective length of database: 297
Effective search space:   117909
Effective search space used:   117909
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 (21.7 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