GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cysK in Sinorhizobium meliloti 1021

Align cysteine synthase (EC 2.5.1.47) (characterized)
to candidate SMc01174 SMc01174 cysteine synthase A

Query= BRENDA::A0A0F6AQU1
         (342 letters)



>FitnessBrowser__Smeli:SMc01174
          Length = 361

 Score =  536 bits (1381), Expect = e-157
 Identities = 260/338 (76%), Positives = 292/338 (86%)

Query: 4   SVLDTIGNTPLIRLSKASELTGCDIYGKAEFLNPGQSVKDRAALYIIRDAEKRGLLRPGG 63
           SVL+ IGNTPLIRL   SE TGC+I GKAEFLNPGQSVKDRAAL+IIR AEK G LRPGG
Sbjct: 21  SVLEAIGNTPLIRLKAVSEATGCNILGKAEFLNPGQSVKDRAALWIIRQAEKSGQLRPGG 80

Query: 64  VIVEGTAGNTGIGLTMVAKALGYRTAIVIPETQSQEKKDALRLLGAELIEVPAAPYRNPN 123
           VIVEGTAGNTGIGL +V  ALGYRT IVIPETQSQEKKDALRLLGAEL+EVPA PYRNPN
Sbjct: 81  VIVEGTAGNTGIGLAVVGSALGYRTVIVIPETQSQEKKDALRLLGAELVEVPAVPYRNPN 140

Query: 124 NYVRLSGRLAEQLAKTEPNGAIWANQFDNTVNRQAHIETTAQEIWRDTSDQIDGFVAAVG 183
           NYV++SGRLA QLA+TEPNGAIWANQFDN  NRQAH++TTA EIWRDT  ++DGF+ AVG
Sbjct: 141 NYVKISGRLAAQLAETEPNGAIWANQFDNVANRQAHVDTTAPEIWRDTDGKVDGFICAVG 200

Query: 184 SGGTLAGTAIGLKERNHNIKIALADPHGAALHAFYTTGELKAEGDSITEGIGQGRITANL 243
           SGGTLAG A GL+ RN  IKI +ADP GAAL+ FY  GELK+ G SITEGIGQGRITANL
Sbjct: 201 SGGTLAGVAEGLRARNAAIKIGIADPEGAALYNFYAHGELKSSGSSITEGIGQGRITANL 260

Query: 244 EGFTPDFSYQIPDAEALDILFALVEEEGLCLGGSSGINIAGAIRLAKDLGPGHTIVTVLC 303
           E FTPDF+YQIPDAEA+  +F L+E+EG+C+GGS+GINIAGA+RLA+DLGPGHTIVT+LC
Sbjct: 261 EDFTPDFAYQIPDAEAVPYVFDLIEKEGICVGGSTGINIAGAVRLARDLGPGHTIVTILC 320

Query: 304 DYGNRYQSKLFNPAFLRGKSLPVPRWLEKKTEIDIPFE 341
           DYGNRYQSKLFNP FL  K LPVP WL+  + I +P+E
Sbjct: 321 DYGNRYQSKLFNPDFLTSKGLPVPDWLKTASNIAVPYE 358


Lambda     K      H
   0.316    0.137    0.398 

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: 468
Number of extensions: 8
Number of successful extensions: 1
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: 342
Length of database: 361
Length adjustment: 29
Effective length of query: 313
Effective length of database: 332
Effective search space:   103916
Effective search space used:   103916
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 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