GapMind for Amino acid biosynthesis

 

Alignments for a candidate for CGL in Methylocella silvestris BL2

Align cystathionine gamma-lyase (EC 4.4.1.1) (characterized)
to candidate WP_012589377.1 MSIL_RS01685 cystathionine gamma-synthase

Query= BRENDA::Q5H4T8
         (397 letters)



>NCBI__GCF_000021745.1:WP_012589377.1
          Length = 385

 Score =  318 bits (816), Expect = 1e-91
 Identities = 175/378 (46%), Positives = 228/378 (60%), Gaps = 2/378 (0%)

Query: 16  SLATLAIHGGQSPDPSTGAVMPPIYATSTYAQSSPGEHQGFEYSRTHNPTRFAYERCVAA 75
           +L T+A   G + D + GA  PPIY +ST+A        G EY+RT NPTR      +A 
Sbjct: 6   ALQTIAASNGVAADSAYGAAAPPIYLSSTFAFKGFERPGGHEYTRTSNPTRDLLADTLAK 65

Query: 76  LEGGTRAFAFASGMAATSTVMELLDAGSHVVAMDDLYGGTFRLFERVRRRTAGLDFSFVD 135
           LEGG  A   +SGMAA + +++ ++    V+A  D Y G  RL              FVD
Sbjct: 66  LEGGAGAVTLSSGMAAINLLLDPMERDDLVIAPHDCYSGVQRLLS-AHAAKGHFKVEFVD 124

Query: 136 LTDPAAFKAAIRADTKMVWIETPTNPMLKLVDIAAIAVIARKHGLLTVVDNTFASPMLQR 195
            +D  A   A+  + K++ IETP+NP++++VDI A    A+K G    VDNTF SP LQR
Sbjct: 125 QSDAEAVATALGRNPKLLMIETPSNPLMRVVDIRAFCEAAKKVGAKVAVDNTFLSPALQR 184

Query: 196 PLSLGADLVVHSATKYLNGHSDMVGGIAVVGDNAELAEQMAFLQNSIGGVQGPFDSFLAL 255
           P+ LGAD VVHS TK+LNGHSD+VGG  +    ++ AE+M    N  G    PFDS+L L
Sbjct: 185 PIPLGADFVVHSMTKFLNGHSDVVGGAVICASESD-AEEMRGWANITGVTGSPFDSYLTL 243

Query: 256 RGLKTLPLRMRAHCENALALAQWLETHPAIEKVIYPGLASHPQHVLAKRQMSGFGGIVSI 315
           RGL+TL  R+      A  +A +L+ HP++E V YPGL SHP H LAK Q +GFG ++S 
Sbjct: 244 RGLRTLFPRLERQQRTAETIALFLQQHPSVEAVHYPGLVSHPSHALAKAQQAGFGAMLSF 303

Query: 316 VLKGGFDAAKRFCEKTELFTLAESLGGVESLVNHPAVMTHASIPVARREQLGISDALVRL 375
            + GG  A +R  E   +FTLAESLGGVESL+ HPA MTHAS+    R   GI D L+RL
Sbjct: 304 EVAGGIAAVRRLVESVRIFTLAESLGGVESLIAHPATMTHASMAPEARAAAGIKDNLLRL 363

Query: 376 SVGIEDLGDLRGDLERAL 393
           SVG+E  GDL  DL +AL
Sbjct: 364 SVGLEHEGDLVSDLAQAL 381


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: 459
Number of extensions: 20
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: 397
Length of database: 385
Length adjustment: 31
Effective length of query: 366
Effective length of database: 354
Effective search space:   129564
Effective search space used:   129564
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 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