GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapL in Klebsiella variicola At-22

Align N-acetyldiaminopimelate deacetylase; EC 3.5.1.47 (uncharacterized)
to candidate WP_008805236.1 KVAR_RS14965 amidohydrolase

Query= curated2:Q032G8
         (376 letters)



>NCBI__GCF_000025465.1:WP_008805236.1
          Length = 389

 Score =  187 bits (476), Expect = 3e-52
 Identities = 118/348 (33%), Positives = 180/348 (51%), Gaps = 18/348 (5%)

Query: 5   IEIRRQLHQIPEIGLEEHKTQKYLLTIIHQIIQNKSFIQVETWQTGILVYLKGSQGQKTI 64
           I +RRQ HQ PEIG EEH+T   +  ++ +       +      TG++  L+   G+K +
Sbjct: 17  IALRRQFHQQPEIGFEEHQTSNEVARLLGEWGYE---VHRGLAGTGVVGTLRVGHGKKRL 73

Query: 65  GWRTDIDGLPVEELTNLPFASK-NGRMHACGHDIHMTVALGLLEKLSES-QPKNNLLFLF 122
           G R D+D LP++E +  P+AS+ +GR H CGHD H T  L   E L+ + Q    L  +F
Sbjct: 74  GLRADMDALPMQERSGKPWASQVDGRFHGCGHDGHTTTLLYAAEYLARTRQFTGTLQLIF 133

Query: 123 QPAEENEAGGKLMYDGGAFKNWLPDEFYGLHVRPDLKVGDIATNEQTLFAGTCEVELTFV 182
           QPAEE   GG++M + G F  +  D  +GLH  P   +G I   +  + A +  + +   
Sbjct: 134 QPAEELLYGGRVMVEDGLFDRFPCDAIFGLHNMPGQPLGKIGLRDGAMMASSDTLHIEVK 193

Query: 183 GTGGHAAFPHTANDALVAAAYFVTQVQTIVSRNVDPLDSAVVTFGKMEAGTTNNIIAERA 242
           G GGH A P    DA + A +    +Q+IVSRN+ P + AVVT G ++AG   NII +  
Sbjct: 194 GVGGHGAVPEHTVDATLVACHITLALQSIVSRNITPFEPAVVTVGSIQAGHAPNIINDHV 253

Query: 243 FLHGTIRSLTQEVNELTQKRLTELAKGVAQSFDMTIDLKLKQGGYLPVENNPKLAKELMD 302
            +  T+R+L ++V E   +R+ ++A   A+SF+ T  L    G   PV  N   A  ++ 
Sbjct: 254 LMKLTVRTLNEQVRETVLQRIHDIAVAQAESFNATATLTHVNGS--PVLRNDPAANAMV- 310

Query: 303 FFRNETKANLI------DIAPAMTGEDFGYLLSKIP-GVMFWLGINSE 343
               E   +L       ++ P M  EDF ++L + P G  F +G   E
Sbjct: 311 ---REVATSLFGAEQVGEVKPFMGSEDFAFMLEQHPHGSYFTIGAGDE 355


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: 373
Number of extensions: 20
Number of successful extensions: 4
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: 389
Length adjustment: 30
Effective length of query: 346
Effective length of database: 359
Effective search space:   124214
Effective search space used:   124214
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 10 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