GapMind for Amino acid biosynthesis

 

Alignments for a candidate for serA in Shewanella oneidensis MR-1

Align Phosphoglycerate dehydrogenase (EC 1.1.1.95) (characterized)
to candidate 199775 SO0585 D-isomer specific 2-hydroxyacid dehydrogenase family protein (NCBI ptt file)

Query= reanno::SB2B:6938941
         (308 letters)



>FitnessBrowser__MR1:199775
          Length = 311

 Score =  379 bits (974), Expect = e-110
 Identities = 184/311 (59%), Positives = 235/311 (75%), Gaps = 3/311 (0%)

Query: 1   MRHKLLLLTRENERYRSLLASCHLPELELLDDNPANIRLADIWLAEPGLAAPLVNHASGL 60
           M HKLLLLT+ NE+YR L+ +  LP LELLDDNPANI  A+IWLAEP LAAPL+ HA  L
Sbjct: 1   MGHKLLLLTKVNEQYRQLIEAQQLPGLELLDDNPANISQANIWLAEPKLAAPLLPHAKQL 60

Query: 61  RWMQSTFAGVDLLVKPRQRRDYLLTNVRGIFGPLMSEYLFGYLLARQREHDLYKSQQQQK 120
           +W+QS+FAG+D L+ PR R+DY LTN++GIFGPLMSEYLFGYLLA  R H  Y+ QQQQK
Sbjct: 61  QWLQSSFAGIDALMGPRARKDYQLTNIKGIFGPLMSEYLFGYLLAHVRGHHFYQQQQQQK 120

Query: 121 LW-LPGSYK--TLQGSELLLLGTGSIAKHLAQTAKHFGMKVAGINRSAKATEGFDEVATL 177
            W + G+ +  +LQG  LL+LGTGSIA+H+ +TAKHFGM V G+NRSA+  EGFD +  L
Sbjct: 121 YWQVQGAMRHTSLQGMRLLILGTGSIAQHVTKTAKHFGMHVTGVNRSAREVEGFDVILPL 180

Query: 178 EALPTLMARADAIASILPSTEATRGILNENILARMKPDAVLFNLGRGDVLDLDALERQLR 237
             L   + ++D + ++LPST  TR +LNE++LA++K DA+L N+GRGD LDLDAL  QL 
Sbjct: 181 SQLAQALGQSDVVTNLLPSTPETRQLLNESMLAKLKADAILMNVGRGDALDLDALNAQLI 240

Query: 238 QHPQQQAVLDVFNQEPLPEDHPIWGLGNVIVTPHIAAPSFPEQVAEIFSSNYHKFLLGET 297
            HP QQA+LDVF QEPLP  HPIW   N I+TPHI+APS PEQ+  IF  NY +++  + 
Sbjct: 241 AHPAQQAILDVFMQEPLPATHPIWERTNAIITPHISAPSHPEQIVSIFCDNYRRYIAAKP 300

Query: 298 LSHRVNFERGY 308
           L ++V+F +GY
Sbjct: 301 LQNQVDFTQGY 311


Lambda     K      H
   0.320    0.137    0.404 

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: 358
Number of extensions: 13
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: 308
Length of database: 311
Length adjustment: 27
Effective length of query: 281
Effective length of database: 284
Effective search space:    79804
Effective search space used:    79804
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: 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