GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysA in Azospirillum brasilense Sp245

Align Diaminopimelate decarboxylase; DAP decarboxylase; DAPDC; EC 4.1.1.20 (characterized)
to candidate AZOBR_RS00105 AZOBR_RS00105 ornithine decarboxylase

Query= SwissProt::B4XMC6
         (405 letters)



>FitnessBrowser__azobra:AZOBR_RS00105
          Length = 378

 Score =  130 bits (326), Expect = 8e-35
 Identities = 116/367 (31%), Positives = 177/367 (48%), Gaps = 25/367 (6%)

Query: 9   QTHKTPFYLYDFDKIKQAFLNYKEAFKGRKSLICYALKANSNLSILSLLAHLESGADCVS 68
           Q  +TP  + D D ++  + + +EA    K  I YA+KAN    IL LL  L S  D  S
Sbjct: 12  QRPQTPCLVVDLDVVEANYHDLEEALPDAK--IFYAVKANPAPEILGLLTRLGSAFDTAS 69

Query: 69  IGEIQRALKAGIKPYRIVFSGVGKSAFEIEQALKLNILFLNVESFMELKTIETIAQSLGI 128
           + EIQ  L AG  P RI +    K   +I +A +L +     +S  EL+ I   A     
Sbjct: 70  VPEIQMVLAAGCAPERISYGNTIKKEADIRRAFELGVRLFAFDSEAELEKIARAAPG--- 126

Query: 129 KARISIRINPNIDAKTHPYISTGLKENKFGVGEKEALEMFLWAKKSAFLEPVSVHFHIGS 188
            AR+  RI  + +    P         KFG     A E+ L AK    + P  V FH+GS
Sbjct: 127 -ARVFCRILTSGEGAEWPL------SRKFGCDLAMARELLLKAKGMNVV-PYGVSFHVGS 178

Query: 189 QLLDLEPIIEASQKVAKIAKSLIALGIDLRFFDVGGGIGVSYENEETIKLYDYAQGILNA 248
           Q  DL     A  +VA++ + L  LG+DL   ++GGG    Y   +  +   Y Q I  +
Sbjct: 179 QQKDLMQWDHAIFQVAQLFRELEVLGVDLGMINLGGGFPTRYRT-DVPETTAYGQAIFES 237

Query: 249 LQ---GLDL-TIICEPGRSIVAESGELITQ-VLYEKKAQN--KRFVIVDAGMNDFLRPSL 301
           L+   G  L   I EPGRS+V  +G + ++ VL  +K+ N  KR+V +D G    L  ++
Sbjct: 238 LRTHFGNRLPEAIVEPGRSMVGNAGIIESEVVLVSRKSANDVKRWVYLDIGKFSGLAETM 297

Query: 302 YHA-KHAIRVITPSKGREISPCDVVGPVCESSDTFLKDAH--LP-ELEPGDKIAIEKVGA 357
             A ++ I+V+      +     + GP C+S+D   + A   LP +L+ GD++ I   GA
Sbjct: 298 DEAIQYPIQVMGDDGEGDSEAVVLAGPTCDSADVLYERAEYKLPMDLKAGDRVRIHATGA 357

Query: 358 YGSSMAS 364
           Y ++ ++
Sbjct: 358 YTTTYSA 364


Lambda     K      H
   0.319    0.138    0.389 

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: 326
Number of extensions: 15
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: 405
Length of database: 378
Length adjustment: 31
Effective length of query: 374
Effective length of database: 347
Effective search space:   129778
Effective search space used:   129778
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