GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PSSH in Paraburkholderia atlantica CCGE1002

Align O-phosphoserine sulfhydrylase monomer (EC 2.5.1.47; EC 2.5.1.65) (characterized)
to candidate WP_013090134.1 BC1002_RS11110 cysteine synthase CysM

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



>NCBI__GCF_000092885.1:WP_013090134.1
          Length = 300

 Score =  253 bits (647), Expect = 3e-72
 Identities = 136/301 (45%), Positives = 201/301 (66%), Gaps = 8/301 (2%)

Query: 1   MIYDNILETIGNTPLVRINHLNPNPKVQ-----MYAKLEGFNPTGSVKDRIALKMIEQAE 55
           M Y  I +T+GNTPLV++  L P+ +++     + AKLEG NP GSVKDR AL MI++AE
Sbjct: 1   MAYKTIEDTVGNTPLVQLVRL-PDDEIRSRNNVILAKLEGNNPAGSVKDRPALSMIKKAE 59

Query: 56  AEGKLHPGSTIIEATSGNTGIGLAMIGRVKGYNVIIVMSEGVSIERRKMIKAFGAEIILT 115
           A G++ PG T+IE+TSGNTGI LAM   V+GY ++++M E +S+ERR+ + A+GAEIILT
Sbjct: 60  ARGRIKPGDTLIESTSGNTGIALAMAAAVRGYKMVLIMPEDLSVERRQSMAAYGAEIILT 119

Query: 116 DKKLGTDGAIRKVAELVKENPGKYFNPNQFSNEYNKIAHYKTTAEEIWAQTKGTVTHFVA 175
             K G + A R +AE ++   GK    +QF+N  N  +H + T  EIW  T+G +THFV+
Sbjct: 120 PVKGGMEYA-RDLAEQMQRE-GKGIILDQFANPDNPASHIEGTGPEIWRDTEGRITHFVS 177

Query: 176 AVGTSGTLMGVGKNLREKNPEIKIIEAQPTKGHYIQGLKSMEEAIVPAIYQADKIDEHIL 235
           ++GT+GT+MGV   L+ +N +I+II AQP +G  I G++   EA +P I+   ++D    
Sbjct: 178 SMGTTGTIMGVSTYLKTQNQQIEIIGAQPEEGSRIPGIRKWPEAYLPKIFDRSRVDRVEN 237

Query: 236 IESEEAFAKAREIVAQEGIFIGMSSGAAMLAAQKLAEKIDSGVIVVLFADRGEKYLSTKL 295
           +    A A AR + + EGIF G+SSG A   A ++A ++++  IV +  DRG++YLST +
Sbjct: 238 VSQSAAEAMARRLASVEGIFAGISSGGACEVALRIARQVENATIVFIVCDRGDRYLSTGV 297

Query: 296 F 296
           F
Sbjct: 298 F 298


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: 274
Number of extensions: 12
Number of successful extensions: 3
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: 300
Length adjustment: 27
Effective length of query: 272
Effective length of database: 273
Effective search space:    74256
Effective search space used:    74256
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