GapMind for Amino acid biosynthesis

 

Alignments for a candidate for CBS in Clostridium kluyveri DSM 555

Align cystathionine β-synthase (O-acetyl-L-serine) monomer (EC 4.2.1.22; EC 2.5.1.134; EC 2.5.1.47) (characterized)
to candidate WP_012101376.1 CKL_RS04935 cysteine synthase A

Query= metacyc::HP_RS00545-MONOMER
         (306 letters)



>NCBI__GCF_000016505.1:WP_012101376.1
          Length = 303

 Score =  289 bits (739), Expect = 6e-83
 Identities = 155/305 (50%), Positives = 200/305 (65%), Gaps = 3/305 (0%)

Query: 1   MMIITTMQDAIGRTPVFKFTNKDYPIPLNSAIYAKLEHLNPGGSVKDRLGQYLIGEGFKT 60
           M+    +++ +G TP+ K  N +  +     I+AKLE  NPGGSVKDR+G Y+I    K 
Sbjct: 1   MVYYNDIKEMVGNTPILKLNNLN--VKREIGIFAKLESFNPGGSVKDRIGLYMIDSAEKK 58

Query: 61  GKITSKTTIIEPTAGNTGIALALVAIKHHLKTIFVVPEKFSTEKQQIMRALGALVINTPT 120
           G +    TI+E TAGNTG+ +AL A+    K IFVVPEKFS EKQ +M+ALGA +INTP 
Sbjct: 59  GLLNKGYTIVEATAGNTGLGIALGALNRGYKVIFVVPEKFSQEKQILMKALGAEIINTPK 118

Query: 121 SEGISGAIKKSKELAESIPDSYLPLQFENPDNPAAYYHTLAPEIVQELGTNLTSFVAGIG 180
            EG+ GAI+KS+EL   IP+S    QFEN DNP A+Y T  PEI  ++  N+   VAG G
Sbjct: 119 EEGMLGAIEKSQELLRDIPNSISLKQFENEDNPKAHYLTTGPEIYMDMEGNIDYLVAGAG 178

Query: 181 SGGTFAGTARYLKERIPAIRLIGVEPEGSILNGGEPGPHEIEGIGVEFIPPFFENLDIDG 240
           SGGTF G A+YLKE+   I+ I V+PEGS + GG  G + IEGIG  FIP   +   +D 
Sbjct: 179 SGGTFTGVAQYLKEKNKNIKSILVDPEGSTMGGGTEGCYGIEGIGNNFIPETMDMGLVDK 238

Query: 241 FETISDEEGFSYTRKLAKKNGLLVGSSSGAAFVAALKEAQRLPEGSQVLTIFPDVADRYL 300
              ++DEE F   RKLA+K GL+VGSSSGAA V ALK AQ + +G+ ++ +FPD  DRY 
Sbjct: 239 IIKVNDEEAFHMVRKLAEKEGLIVGSSSGAALVGALKLAQSIDKGN-IVVVFPDRGDRYF 297

Query: 301 SKGIY 305
           SK IY
Sbjct: 298 SKNIY 302


Lambda     K      H
   0.316    0.137    0.389 

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: 299
Number of extensions: 14
Number of successful extensions: 2
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: 306
Length of database: 303
Length adjustment: 27
Effective length of query: 279
Effective length of database: 276
Effective search space:    77004
Effective search space used:    77004
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: 41 (21.6 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