GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gatD in Shewanella sp. ANA-3

Align Glutamyl-tRNA(Gln) amidotransferase subunit D; Glu-ADT subunit D; EC 6.3.5.- (uncharacterized)
to candidate 7024785 Shewana3_1963 cytoplasmic asparaginase I (RefSeq)

Query= curated2:O59132
         (438 letters)



>FitnessBrowser__ANA3:7024785
          Length = 337

 Score =  156 bits (395), Expect = 8e-43
 Identities = 111/339 (32%), Positives = 174/339 (51%), Gaps = 21/339 (6%)

Query: 99  TGGTIASRIDYETGAVYPAFTAEELAKAVPEIFEIANIKPKLLFN-----IFSEDMKPKH 153
           TGGTI  +      A    F  +   +++PE +   +  P+ + +     I S +M P  
Sbjct: 11  TGGTIGMQKTANGFAPVAGFLTQ-CVQSMPEFYH--DEMPEFVIHEYCPLIDSSNMAPTD 67

Query: 154 WIKIAHEVAKSLNSGDSGVVVAHGTDTMGYTAAALSFMLRDLGKPVILVGAQRSSDRPSS 213
           W  IA ++  + +  D G V+ HGTDTM YTA+ALSFML+ L KPVI+ G+Q    +  S
Sbjct: 68  WQMIADDIKANYDKYD-GFVILHGTDTMAYTASALSFMLQGLSKPVIVTGSQIPLAQLRS 126

Query: 214 DAAMNLICSVRMSTS-DVAEVMVVMHGETGDTYCLAHRGTKVRKMHTSRRDAFRSINDVP 272
           D   NL+ S+ ++ +  VAEV +  + +         RG +  K H    DAF S N   
Sbjct: 127 DGQTNLLNSLYIAANYPVAEVCLFFNNKL-------FRGNRSTKAHADGFDAFASPNFPL 179

Query: 273 IAKVWPNGKIEFLRDDYRRRSDSEVWVDDKLEEKVALVKVYPGISSEIIEFFIDKGYRGI 332
           + +     KI          SD  + V +   + V +V +YPGIS++I E  + +  + +
Sbjct: 180 LLEA--GIKINLRAGKIATPSDKPLEVANISPQPVGVVTLYPGISTQIFENILQQPVKAL 237

Query: 333 VIEGTGLGHTPND--IIPSIQRATEEGIAVCMTSQCIYGRVNLNVYATGRRLLKAGVIPC 390
           ++   G+G+ P D  ++ ++++A E GI +   +QC  G+VN+  YATG  L KAGVI  
Sbjct: 238 ILLTFGVGNAPQDAALLDTLKQADERGIVLVNLTQCFQGKVNMGGYATGNALAKAGVISG 297

Query: 391 EDMLPETAYVKLMWVLGHTQDLEEVRRMMLTNYAGEITP 429
            DM  E A  KL ++L       E++  ML N  GE++P
Sbjct: 298 ADMTIEAALAKLHYLLSKNLKPSEIKTAMLQNLVGELSP 336


Lambda     K      H
   0.320    0.138    0.403 

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: 344
Number of extensions: 14
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: 438
Length of database: 337
Length adjustment: 30
Effective length of query: 408
Effective length of database: 307
Effective search space:   125256
Effective search space used:   125256
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 (21.8 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