GapMind for Amino acid biosynthesis

 

Alignments for a candidate for Mt_cysM in Caulobacter crescentus NA1000

Align [CysO sulfur-carrier protein]-thiocarboxylate-dependent cysteine synthase (EC 2.5.1.113); O-phosphoserine sulfhydrylase (EC 2.5.1.65) (characterized)
to candidate CCNA_01493 CCNA_01493 cysteine synthase

Query= BRENDA::P9WP53
         (323 letters)



>FitnessBrowser__Caulo:CCNA_01493
          Length = 332

 Score =  145 bits (366), Expect = 1e-39
 Identities = 112/324 (34%), Positives = 157/324 (48%), Gaps = 33/324 (10%)

Query: 1   MTRYDSLLQALGNTPLVGLQRLSPRWDDGRDGPHVRLWAKLEDRNPTGSIKDRPAVRMIE 60
           M+   S+L A+GNTPL+ L R S       +     +  K E  NP  S+KDR A+ +I 
Sbjct: 1   MSALPSVLDAIGNTPLIRLARAS-------EATGCEILGKAEFMNPGQSVKDRAALAIIR 53

Query: 61  QAEADGLLRPGATILEPTSGNTGISLAMAARLKGYRLICVMPENTSVERRQLLELYGAQI 120
            AEA GLLRPG  I+E T+GNTGI LAM A   GY+   V+P   S E++  + L GA++
Sbjct: 54  DAEAKGLLRPGGRIVEGTAGNTGIGLAMVASALGYKTTIVIPRTQSQEKKDAIRLLGAEL 113

Query: 121 I------FSAAEGGSNTAVATAKELAATNPSWVM-LYQYGNPANTDSHYCGTGPELLADL 173
           +      +S  +     +   A+ELA T P  V+   Q+ N AN D+HY  TGPE+    
Sbjct: 114 VEVDAVPYSNPDNYVRYSGRLAEELARTEPHGVIWANQFDNTANRDAHYHTTGPEIFDQT 173

Query: 174 P-EITHFVAGLGTTGTLMGTGRFLREHVANVKIVAAEPRYGEGVYALRNMDE-----GFV 227
             ++  F+  +G+ GTL G    LRE    V+I  A+P YG  +YA     E       +
Sbjct: 174 SGKVDGFICAVGSGGTLAGVAAALRERKPGVRIGLADP-YGAALYAWYKDGELKSEGSSI 232

Query: 228 PELYDPEILTARYSVGAVDAVRRTR---------ELVHTEGIFAGISTGAVLHAALGVGA 278
            E      +TA     A+D   R           +LV  EG+  G S G  +  A+ +  
Sbjct: 233 SEGIGQGRITANLEGLAIDDPFRVSDQEMLEVLYDLVQHEGLCLGGSAGINVAGAIKL-- 290

Query: 279 GALAAGERADIALVVADAGWKYLS 302
            A A G    I  V+ D G +Y S
Sbjct: 291 -ATAMGPGHTIVTVLCDHGSRYQS 313


Lambda     K      H
   0.317    0.134    0.398 

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: 293
Number of extensions: 18
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: 323
Length of database: 332
Length adjustment: 28
Effective length of query: 295
Effective length of database: 304
Effective search space:    89680
Effective search space used:    89680
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 Apr 09 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