GapMind for Amino acid biosynthesis

 

Alignments for a candidate for PSSH in Carboxydothermus pertinax Ug1

Align O-phosphoserine sulfhydrylase monomer (EC 2.5.1.47; EC 2.5.1.65) (characterized)
to candidate WP_075859204.1 cpu_RS06395 cysteine synthase A

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



>NCBI__GCF_001950255.1:WP_075859204.1
          Length = 306

 Score =  266 bits (680), Expect = 4e-76
 Identities = 144/304 (47%), Positives = 197/304 (64%), Gaps = 10/304 (3%)

Query: 2   IYDNILETIGNTPLVRINHLNPNPKVQMYAKLEGFNPTGSVKDRIALKMIEQAEAEGKLH 61
           IY +I E IG TPL+++  ++ + K  + AKLE FNP GSVKDRIA  MI+ AE +G L 
Sbjct: 3   IYQDITELIGKTPLLKLKRVSKDAKATVVAKLEYFNPGGSVKDRIAYNMIKAAEEKGLLD 62

Query: 62  PGSTIIEATSGNTGIGLAMIGRVKGYNVIIVMSEGVSIERRKMIKAFGAEIILTDKKLGT 121
             + IIE TSGNTGIGLAM+   +GY +II M E +S+ERR ++KA+GAEI+LT  +LG 
Sbjct: 63  KDTVIIEPTSGNTGIGLAMVAAARGYRLIITMPETMSVERRMLLKAYGAEIVLTPGELGM 122

Query: 122 DGAIRKVAELVKENPGKYFNPNQFSNEYNKIAHYKTTAEEIWAQTKGTVTHFVAAVGTSG 181
            GA+ K  EL KE P K F P QF N  N   H +TTA EIW  T G V   V  VGT G
Sbjct: 123 TGAVNKALELAKEYP-KSFIPQQFENPANPEIHRQTTALEIWEDTDGKVDIVVGGVGTGG 181

Query: 182 TLMGVGKNLREKNPEIKIIEAQPTKGHYIQG-------LKSMEEAIVPAIYQADKIDEHI 234
           T+ GVG+ L+ K PE+KII  +P     + G       ++ +    +P +   D IDE I
Sbjct: 182 TITGVGEVLKAKKPEVKIIAVEPAASPVLSGGKPGPHKIQGIGAGFIPKVLNLDVIDEII 241

Query: 235 LIESEEAFAKAREIVAQEGIFIGMSSGAAMLAAQKLAEKIDS--GVIVVLFADRGEKYLS 292
            +E+E+AFA A+E+  +EG+ +G+SSGAA+ AA ++A++ ++   +IVV+  D GE+YLS
Sbjct: 242 RVENEDAFATAKELAREEGVLVGISSGAALWAALEVAKRPENEGKLIVVVLPDTGERYLS 301

Query: 293 TKLF 296
           T LF
Sbjct: 302 TPLF 305


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: 291
Number of extensions: 13
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: 306
Length adjustment: 27
Effective length of query: 272
Effective length of database: 279
Effective search space:    75888
Effective search space used:    75888
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.

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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