GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Cupriavidus basilensis 4G11

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate RR42_RS27930 RR42_RS27930 amidohydrolase

Query= curated2:Q032G8
         (376 letters)



>FitnessBrowser__Cup4G11:RR42_RS27930
          Length = 387

 Score =  183 bits (464), Expect = 8e-51
 Identities = 115/341 (33%), Positives = 177/341 (51%), Gaps = 14/341 (4%)

Query: 6   EIRRQLHQIPEIGLEEHKTQKYLLTIIHQIIQNKSFIQVETWQTGILVYLKGSQGQKTIG 65
           E+R ++H  PE+G +  +T +    ++ +   +   +       G++  LK   G +TIG
Sbjct: 14  EVRHRIHAHPELGADVPRTAEMAAALLREWGYSVHTLGGH----GLVAQLKVGNGARTIG 69

Query: 66  WRTDIDGLPVEELTNLPFASK-NGRMHACGHDIHMTVALGLLEKLSESQPKNNLL-FLFQ 123
            R D+D LP++E T LP+AS+  GRMHACGHD H    L   E L+ ++  +  L  +FQ
Sbjct: 70  IRADMDALPLQERTGLPYASQVAGRMHACGHDGHTATLLAAAEYLAATRHFDGTLNLIFQ 129

Query: 124 PAEENEAGGKLMYDGGAFKNWLPDEFYGLHVRPDLKVGDIATNEQTLFAGTCEVELTFVG 183
           P EE   G   M + G F+ +  D  Y  H  P L VG        +   +    +TF G
Sbjct: 130 PDEEGMTGALAMMNDGLFERFPCDAIYAFHNAPGLPVGMAVVQSGPMGGSSDRATITFRG 189

Query: 184 TGGHAAFPHTANDALVAAAYFVTQVQTIVSRNVDPLDSAVVTFGKMEAGTTNNIIAERAF 243
            GGH A PH A D  +A A  V  +Q IV+RNV P+D+AV++ G+M+AG+T NII E A 
Sbjct: 190 KGGHGAMPHRATDPTLALASTVVALQGIVARNVAPVDAAVISVGEMQAGSTYNIIPETAT 249

Query: 244 LHGTIRSLTQEVNELTQKRLTELAKGVAQSFDMTIDL---KLKQGGYLPVENNPKLAKEL 300
           L  ++R+   EV +L + R+ E+    A S  + +D+   +L       VE      + +
Sbjct: 250 LKLSVRATVAEVRDLLETRIREVVTHQAASCGVAVDIAYERLAPAICNTVEETAIARQAV 309

Query: 301 MDFFRNETKANLIDIAPAMT--GEDFGYLLSKIPGVMFWLG 339
                N+    +I + P+M    EDF ++L ++PG  F LG
Sbjct: 310 ASVLGND---KVIQVPPSMQMGSEDFAWMLERMPGCYFALG 347


Lambda     K      H
   0.319    0.136    0.396 

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: 317
Number of extensions: 13
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: 376
Length of database: 387
Length adjustment: 30
Effective length of query: 346
Effective length of database: 357
Effective search space:   123522
Effective search space used:   123522
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