GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gatD in Escherichia coli BW25113

Align Glutamyl-tRNA(Gln) amidotransferase subunit D; Glu-ADT subunit D; EC 6.3.5.- (uncharacterized)
to candidate 15885 b1767 cytoplasmic asparaginase I (NCBI)

Query= curated2:A5UK11
         (436 letters)



>FitnessBrowser__Keio:15885
          Length = 338

 Score =  160 bits (404), Expect = 7e-44
 Identities = 112/343 (32%), Positives = 176/343 (51%), Gaps = 20/343 (5%)

Query: 90  KQNISIISTGGTVS---SIIDYRTGAVHPKFTAADLIKAN-PELLDYANYNVKALYNILS 145
           K++I +  TGGT+    S   Y   + H +   A + + + PE+ D+  +    L +  S
Sbjct: 3   KKSIYVAYTGGTIGMQRSEQGYIPVSGHLQRQLALMPEFHRPEMPDFTIHEYTPLMD--S 60

Query: 146 ENMQPKYWVEAAESIANDISDGSDGIVIAHGTDTLHYTAAALSFMLKT-PVPIVITGAQR 204
            +M P+ W   AE I     D  DG VI HGTDT+ YTA+ALSFML+    P+++TG+Q 
Sbjct: 61  SDMTPEDWQHIAEDIKAHYDD-YDGFVILHGTDTMAYTASALSFMLENLGKPVIVTGSQI 119

Query: 205 SSDRPSSDANMNLIDSV-VAAKSDIAEVSVCMHGSLNDSYTYLHKGTKVRKMHTSRRDTF 263
                 SD  +NL++++ VAA   I EV++  +  L       ++G +  K H    D F
Sbjct: 120 PLAELRSDGQINLLNALYVAANYPINEVTLFFNNRL-------YRGNRTTKAHADGFDAF 172

Query: 264 RSINYEPIAKIENHSVDINPNYRYTKRNENELEVNSAVEEKVGLIKSFPGICEELIEYHI 323
            S N  P+ +   H   +N         E EL V+    + +G++  +PGI  +++   +
Sbjct: 173 ASPNLPPLLEAGIHIRRLNTPP--APHGEGELIVHPITPQPIGVVTIYPGISADVVRNFL 230

Query: 324 DKGYKGLVIEGTGLGHVPDK--LITPLARAHDENIPVVMTSQCLYGRVNMNVYSTGREIL 381
            +  K L++   G+G+ P     +  L  A D  I VV  +QC+ G+VNM  Y+TG  + 
Sbjct: 231 RQPVKALILRSYGVGNAPQNKAFLQELQEASDRGIVVVNLTQCMSGKVNMGGYATGNALA 290

Query: 382 NAGVISGRDMTPETAYVKLSWVLGQTNDIGEVAKLMNKNIAGE 424
           +AGVI G DMT E    KL ++L Q  D   + K M++N+ GE
Sbjct: 291 HAGVIGGADMTVEATLTKLHYLLSQELDTETIRKAMSQNLRGE 333


Lambda     K      H
   0.313    0.132    0.373 

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: 375
Number of extensions: 24
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: 436
Length of database: 338
Length adjustment: 30
Effective length of query: 406
Effective length of database: 308
Effective search space:   125048
Effective search space used:   125048
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 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