GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serA in Pseudomonas putida KT2440

Align phosphoglycerate dehydrogenase (EC 1.1.1.95) (characterized)
to candidate PP_1707 PP_1707 D-isomer specific 2-hydroxyacid dehydrogenase family protein

Query= BRENDA::O58256
         (333 letters)



>FitnessBrowser__Putida:PP_1707
          Length = 316

 Score =  152 bits (384), Expect = 1e-41
 Identities = 108/326 (33%), Positives = 169/326 (51%), Gaps = 20/326 (6%)

Query: 1   MRPKV----GVLLKMKREALEEL----KKYADVEIILYPSGEELKGVIGRFDGIIVSPTT 52
           M+P+V     +L+   RE LE+L    + Y   +   Y S        G   G+I    T
Sbjct: 1   MKPEVLQLSPILIPQIRERLEQLFTVHRYYEQADKEAYVSQHA-----GNIRGVITGGHT 55

Query: 53  KITREVLENAERLKVISCHSAGYDNIDLEEATKRGIYVTKVSGLLSEAVAEFTVGLIINL 112
            I++ ++     L+VI+ +  G D +DL  A  RGI VT   G L+E VA+  +GL+I L
Sbjct: 56  GISQALMARLPNLEVIAVNGVGTDAVDLAYARDRGIQVTATIGALTEDVADLAIGLLIGL 115

Query: 113 MRKIHYADKFIRRGEWESHAKIWTGFKRIESLYGKKVGILGMGAIGKAIARRLIPFGVKL 172
            R I   D+F+R G W +             + G +VGI+GMG +G+A+A+R   FG  +
Sbjct: 116 CRGICTGDRFVRAGRWATSTTPLAPLPLARQVSGMRVGIVGMGRVGRAVAQRAAAFGCPI 175

Query: 173 YYWSRHRKVNVEKELKARYMDIDELLEKSDIVILALPLTRDTYHIINEERVKKLEGK-YL 231
            Y +  + ++V    +A   D+ +L + SD +ILA    +    +IN + ++ L  + YL
Sbjct: 176 RY-TDLQALDVPYGFEA---DLLQLAKDSDALILAAAADKGE-ALINRDVLQALGSEGYL 230

Query: 232 VNIGRGALVDEKAVTEAIKQGKLKGYATDVFEKEPVREHELFKYEWETVLTPHYAGLALE 291
           +NI RG LVDE A+  A++ G++ G A DVF  EP     LF+ E + VL PH A   ++
Sbjct: 231 INIARGKLVDEPALIAALQAGEIGGAALDVFADEPRAPEALFERE-DVVLQPHRASATVQ 289

Query: 292 AQEDVGFRAVENLLKVLRGEVPEDLV 317
            +  +G   V +L+ V  G  P+ LV
Sbjct: 290 TRTRMGEMVVASLVDVFAGRTPQGLV 315


Lambda     K      H
   0.319    0.139    0.393 

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: 242
Number of extensions: 11
Number of successful extensions: 2
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: 333
Length of database: 316
Length adjustment: 28
Effective length of query: 305
Effective length of database: 288
Effective search space:    87840
Effective search space used:    87840
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: 48 (23.1 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