GapMind for Amino acid biosynthesis

 

Alignments for a candidate for CGL in Methylococcus capsulatus Bath

Align cystathionine gamma-lyase (EC 4.4.1.1) (characterized)
to candidate WP_081423433.1 MCA_RS12205 O-succinylhomoserine sulfhydrylase

Query= BRENDA::Q5H4T8
         (397 letters)



>NCBI__GCF_000008325.1:WP_081423433.1
          Length = 411

 Score =  318 bits (814), Expect = 2e-91
 Identities = 176/363 (48%), Positives = 232/363 (63%), Gaps = 11/363 (3%)

Query: 38  PIYATSTY--------AQSSPGEHQGFEYSRTHNPTRFAYERCVAALEGGTRAFAFASGM 89
           PI+ATS+Y        A+   G+  G  YSR  NPT   +E  +AALEGG R  A  SGM
Sbjct: 49  PIFATSSYVFASAAEAAERFAGKAAGNIYSRFTNPTVRTFEERLAALEGGERCVAVGSGM 108

Query: 90  AA-TSTVMELLDAGSHVVAMDDLYGGTFRLFERVRRRTAGLDFSFVDLTDPAAFKAAIRA 148
           AA  ST   LL AG HVV    ++G T  LF+    +  G+  +FV LTD   + AAIR 
Sbjct: 109 AAIASTAFGLLKAGDHVVCSRSVFGNTTLLFQNYLAKF-GVPTTFVGLTDYDGWAAAIRP 167

Query: 149 DTKMVWIETPTNPMLKLVDIAAIAVIARKHGLLTVVDNTFASPMLQRPLSLGADLVVHSA 208
           +T+ ++IETP+NP+ ++ DI  +A IA   G L VVDN F +P LQRPL+LGAD+V+HSA
Sbjct: 168 ETRFLFIETPSNPLTEIADIPRLAEIAHSRGCLLVVDNCFCTPALQRPLALGADIVIHSA 227

Query: 209 TKYLNGHSDMVGGIAVVGDNAELAEQMAFLQNSIGGVQGPFDSFLALRGLKTLPLRMRAH 268
           TKYL+G    VGG  V G     AE   FL+   G    PF++++ L+GL+TL LRM+AH
Sbjct: 228 TKYLDGQGRCVGGAIVGGRELLDAEIYPFLRTG-GPSMSPFNAWVFLKGLETLNLRMKAH 286

Query: 269 CENALALAQWLETHPAIEKVIYPGLASHPQHVLAKRQMSGFGGIVSIVLKGGFDAAKRFC 328
           CENAL LA+WLE  P +E+V YPGLASHPQH LA RQ SGFGGIVS  +KGG +AA R  
Sbjct: 287 CENALGLARWLEAQPWVERVHYPGLASHPQHELAARQQSGFGGIVSFEVKGGQEAAWRLI 346

Query: 329 EKTELFTLAESLGGVESLVNHPAVMTHASIPVARREQLGISDALVRLSVGIEDLGDLRGD 388
           + T L ++  +LG  ++ + HPA  TH  +    R   GI+D L+R++VG+E+L D++ D
Sbjct: 347 DSTRLLSITGNLGDAKTTITHPATTTHGRLSPEARAAAGIADGLIRIAVGLENLADIQAD 406

Query: 389 LER 391
           L R
Sbjct: 407 LAR 409


Lambda     K      H
   0.320    0.134    0.391 

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: 477
Number of extensions: 21
Number of successful extensions: 5
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: 397
Length of database: 411
Length adjustment: 31
Effective length of query: 366
Effective length of database: 380
Effective search space:   139080
Effective search space used:   139080
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 (21.8 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 10 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