GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metY in Pseudomonas simiae WCS417

Align O-acetylhomoserine sulfhydrylase (EC:2.5.1.49) (characterized)
to candidate GFF2301 PS417_11735 methionine gamma-lyase

Query= reanno::Korea:Ga0059261_3194
         (402 letters)



>FitnessBrowser__WCS417:GFF2301
          Length = 411

 Score =  253 bits (646), Expect = 7e-72
 Identities = 150/385 (38%), Positives = 220/385 (57%), Gaps = 5/385 (1%)

Query: 18  ATQAIRGG-TARSEWGETSEALFLTSGYAYDCAGDAAARFSGDQQGMTYSRLQNPTVEML 76
           +T+AI  G   +   G     ++L++ +A+  A   AA F+G+  G  Y+R+ NPT+ +L
Sbjct: 11  STRAIHHGYDPKDHHGALVPPIYLSATFAFPTAEYGAACFAGEASGHFYTRISNPTLALL 70

Query: 77  EQRIALLEGAEACRATASGMAAMTAALLCQLSAGDHLIGGRAAFGSCRWLTDTQLPKFGI 136
           E R+A LE  +A  A +SGM A+ A     L  GD +I  +  +G    L    + +FGI
Sbjct: 71  ESRMATLENGDAAVAFSSGMGAIAATFWTLLRPGDEVIVSQTLYGCTFALLHHGIGEFGI 130

Query: 137 ETTVVDARDPQQFIDAIRPNTKVFFFETPANPTMDVVDLKAVCAIARERGIVT-VVDNAF 195
           +   VD  D      A+ P T++ + ETPANP + +VD+ AV A+A ++  VT VVDN +
Sbjct: 131 KVRHVDLTDLTALQAALTPATRMIYCETPANPNLRLVDIAAVAALAHQQPNVTLVVDNTY 190

Query: 196 ATPALQRPMDFGADVVAYSATKMMDGQGRVLAGAVCGTEEFINNTLLPFHRN-TGPTLSP 254
            TP LQRP++ GADVV +SATK + G G + AG     +       L   ++ TG  +SP
Sbjct: 191 CTPYLQRPLELGADVVVHSATKYLSGHGDITAGIAVSNQALAQRIRLQGLKDLTGAVMSP 250

Query: 255 FNAWVVLKGLETLDLRIQRQSENALKVARFLEGR--VPRVNFPGLPSHPQHNLAMSQMAA 312
            +A ++++GL+TL LR+ R   NA  VA  L+    V  V +PGL S PQ+ LA  QM  
Sbjct: 251 QDASLLMRGLKTLALRMDRHCSNAQAVAEALQAHPAVQSVTYPGLRSFPQYELATQQMKM 310

Query: 313 AGPIFSIELDGGRTQAHGLLDALGLIDISNNIGDSRSLMTHPASTTHSGVAEDQRLLMGV 372
            G + + EL GG       ++AL L   + ++GD+ SL  HPAS THS     +R   G+
Sbjct: 311 PGGMIAFELKGGIETGRRFMNALKLFTRAVSLGDAESLAQHPASMTHSTYTPQERAAHGI 370

Query: 373 GEGMLRLNVGLEDPEDLIADLDQAL 397
            EG++RL+VGLED  DL+AD+ QAL
Sbjct: 371 SEGLVRLSVGLEDVADLLADVQQAL 395


Lambda     K      H
   0.319    0.134    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: 375
Number of extensions: 10
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: 402
Length of database: 411
Length adjustment: 31
Effective length of query: 371
Effective length of database: 380
Effective search space:   140980
Effective search space used:   140980
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: 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