GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PSSH in Desulfobacter vibrioformis DSM 8776

Align O-phosphoserine sulfhydrylase monomer (EC 2.5.1.47; EC 2.5.1.65) (characterized)
to candidate WP_035238797.1 Q366_RS10715 cysteine synthase A

Query= metacyc::MONOMER-20568
         (299 letters)



>NCBI__GCF_000745975.1:WP_035238797.1
          Length = 313

 Score =  232 bits (591), Expect = 9e-66
 Identities = 128/301 (42%), Positives = 183/301 (60%), Gaps = 10/301 (3%)

Query: 4   DNILETIGNTPLVRINHLNPNPKVQMYAKLEGFNPTGSVKDRIALKMIEQAEAEGKLHPG 63
           + IL  IG TP+ RI  L  N  + +YAK E  NP GS+KDR+AL +IEQAE +G+L  G
Sbjct: 4   NEILNQIGATPMFRIG-LGGNDDMNIYAKAEYLNPGGSIKDRVALFIIEQAEKKGRLKKG 62

Query: 64  STIIEATSGNTGIGLAMIGRVKGYNVIIVMSEGVSIERRKMIKAFGAEIILTDKKLGTDG 123
            +I+EATSGNTGI +AM+G VKGY+V I+M E +S ER+KMI+A  AE+ILT  +    G
Sbjct: 63  MSIVEATSGNTGIAVAMVGLVKGYDVRIIMPENMSDERKKMIRALNAELILTPPEKNVAG 122

Query: 124 AIRKVAELVKENPGKYFNPNQFSNEYNKIAHYKTTAEEIWAQTKGTVTHFVAAVGTSGTL 183
           A+ K+ E++ E+    F P+QF N  N ++HY +T  EIW    G V  FV+ +G+ GTL
Sbjct: 123 AVEKLKEIMAED-DNIFVPDQFENHDNSMSHYLSTGPEIWKNMNGHVDIFVSGLGSGGTL 181

Query: 184 MGVGKNLREKNPEIKIIEAQPTKGHYIQG-------LKSMEEAIVPAIYQADKIDEHILI 236
           MG GK L+EKNPEI I+  +P     + G       ++ + +  VP+I     ID  I +
Sbjct: 182 MGTGKYLKEKNPEIMIVAVEPKNASALLGHEPGLHKIEGIGDGFVPSIVDTSLIDNVIEV 241

Query: 237 ESEEAFAKAREIVAQEGIFIGMSSGAAMLAAQKLAEKIDSGV-IVVLFADRGEKYLSTKL 295
           + + A    R + +++G  +G+SSGA + AA ++         I  +F D  E+Y ST L
Sbjct: 242 DDDSAVEMTRWLASKQGFLVGISSGANVCAALEMRHLFGKDKNIATIFPDGAERYFSTAL 301

Query: 296 F 296
           F
Sbjct: 302 F 302


Lambda     K      H
   0.315    0.133    0.367 

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: 295
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: 299
Length of database: 313
Length adjustment: 27
Effective length of query: 272
Effective length of database: 286
Effective search space:    77792
Effective search space used:    77792
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: 42 (22.0 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.

Links

Downloads

Related tools

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