GapMind for Amino acid biosynthesis

 

Alignments for a candidate for CGL in Caulobacter crescentus NA1000

Align cystathionine gamma-lyase (EC 4.4.1.1) (characterized)
to candidate CCNA_03271 CCNA_03271 methionine gamma-lyase

Query= BRENDA::Q5H4T8
         (397 letters)



>FitnessBrowser__Caulo:CCNA_03271
          Length = 401

 Score =  320 bits (821), Expect = 4e-92
 Identities = 184/391 (47%), Positives = 232/391 (59%), Gaps = 10/391 (2%)

Query: 12  DRALSLATLAIHGGQSPDPSTGAVMPPIYATSTYAQSSP--------GEHQGFEYSRTHN 63
           D     +T AIH G  P    GA+ PP++ TST+A  S         G  +G  YSR  N
Sbjct: 3   DDQTGFSTRAIHAGYDPADEHGALTPPLHLTSTFAFESAEAGGEMFAGTREGHFYSRISN 62

Query: 64  PTRFAYERCVAALEGGTRAFAFASGMAA-TSTVMELLDAGSHVVAMDDLYGGTFRLFERV 122
           PT    ER +A+LEG   A A ASGM A T+T+   L AG  V+    LYG TF  F R 
Sbjct: 63  PTTDLLERRLASLEGAEAAVATASGMGAITATLWSFLRAGDEVITDQTLYGCTFA-FLRD 121

Query: 123 RRRTAGLDFSFVDLTDPAAFKAAIRADTKMVWIETPTNPMLKLVDIAAIAVIARKHGLLT 182
                G+    VD+T P    AAI   T++V+ ETP NP ++LVDIAAI  IA   G   
Sbjct: 122 GLTRFGVTVKQVDMTRPETLAAAISDQTRIVYFETPANPNMRLVDIAAITRIAHAAGAKV 181

Query: 183 VVDNTFASPMLQRPLSLGADLVVHSATKYLNGHSDMVGGIAVVGDNAELAEQMAFLQNSI 242
           VVDNT+A+P L RPL+LGAD+VVHSATKYL GH D+VGGIA  G       ++  +++  
Sbjct: 182 VVDNTYATPCLTRPLALGADIVVHSATKYLGGHGDLVGGIAAGGIEDMARVRLCGVKDMT 241

Query: 243 GGVQGPFDSFLALRGLKTLPLRMRAHCENALALAQWLETHPAIEKVIYPGLASHPQHVLA 302
           G V  PF +FL LRGLKTL LRM  H ++A A+A+WLE HPA+E+V YPGL S PQ  LA
Sbjct: 242 GAVMSPFTAFLVLRGLKTLSLRMARHSQSAQAVARWLEDHPAVEQVFYPGLQSFPQRDLA 301

Query: 303 KRQMSGFGGIVSIVLKGGFDAAKRFCEKTELFTLAESLGGVESLVNHPAVMTHASIPVAR 362
            RQM+  GG+++  LKGG  A      +  L   A SLG  E+L+ HPA MTH+      
Sbjct: 302 ARQMAAGGGMMAFELKGGHAAGVAMMNRLALIRRAVSLGDAETLIQHPASMTHSPYTPEE 361

Query: 363 REQLGISDALVRLSVGIEDLGDLRGDLERAL 393
           R   GI + +VRLSVG+ED+ D+  DL  AL
Sbjct: 362 RAAAGIGEGMVRLSVGLEDVADILADLAMAL 392


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: 491
Number of extensions: 24
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: 401
Length adjustment: 31
Effective length of query: 366
Effective length of database: 370
Effective search space:   135420
Effective search space used:   135420
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 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