GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cysK in Dinoroseobacter shibae DFL-12

Align O-ureido-L-serine synthase; Cysteine synthase homolog DscD; O-acetylserine sulfhydrylase; EC 2.6.99.3; EC 2.5.1.47 (characterized)
to candidate 3607478 Dshi_0891 cysteine synthase A (RefSeq)

Query= SwissProt::D2Z027
         (324 letters)



>FitnessBrowser__Dino:3607478
          Length = 360

 Score =  306 bits (784), Expect = 5e-88
 Identities = 162/329 (49%), Positives = 212/329 (64%), Gaps = 20/329 (6%)

Query: 4   FNSILDTIGRTPIVRLQRMAPEHTSVYVKVESFNPGGSVKDRLALSVVLDAEAKGLLKPG 63
           ++S+LDT+G TP++R+  +APE   +YVK E FNP  SVKDRLAL+++  AE  G LKPG
Sbjct: 17  YDSVLDTVGNTPVIRINNLAPEGVELYVKAEFFNPAASVKDRLALNIIEAAERAGTLKPG 76

Query: 64  DTIVECTSGNVGIALAMVAAARGYRFVAVMGDTYSVERRKLIRAYGGKLVLFPGHLGSKG 123
            T+VE TSGN GI LAMV A +GY  V  M +++S+ERRKL+R  G K+VL P      G
Sbjct: 77  QTVVEATSGNTGIGLAMVCAQKGYPLVITMAESFSIERRKLMRLLGAKVVLTPRAEKGFG 136

Query: 124 GNLIADELAEKYGWFRARQFDNPANPSYHRETTASEILADFAGKRLDHFVTGFGTTGTLT 183
               A ELAE  GWF A QF+  AN   H  TTA EIL DF G +LD+ VTG+GT GT+T
Sbjct: 137 MYRKAVELAEANGWFLASQFETAANAEMHENTTAQEILGDFEGCKLDYIVTGYGTGGTVT 196

Query: 184 GVGQMLRVARPEVRVVALEPSNAAMLARG----------------EWSPHQIQGLAPNFV 227
           G+G++LR ARPE +++  EP+NA +L  G                 + PH IQG  P+F+
Sbjct: 197 GLGRVLRKARPETKIILTEPANAQLLGSGIAQDRDPNGAPAVSHSAFEPHPIQGWTPDFI 256

Query: 228 PGVLDRSV----IDDLVTMDEVTARDTSRRLAAEEGIFAGISAGATVATALSIAEHAPEG 283
           P VL  S+     D L+ +        +RRLAAEEGI  GIS G+T A +  +A+ APEG
Sbjct: 257 PKVLQESIDQGFYDALLPVAGADGIAWARRLAAEEGILTGISGGSTFAISHEVAKTAPEG 316

Query: 284 TVLLAMLPDTGERYLSTFLFDGVDEGSDD 312
           +V+L MLPDTGERYLST LF+G+ E  ++
Sbjct: 317 SVILCMLPDTGERYLSTPLFEGIVEDMNE 345


Lambda     K      H
   0.319    0.136    0.395 

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: 16
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: 324
Length of database: 360
Length adjustment: 29
Effective length of query: 295
Effective length of database: 331
Effective search space:    97645
Effective search space used:    97645
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: 49 (23.5 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