GapMind for Amino acid biosynthesis

 

Alignments for a candidate for CGL in Pseudomonas fluorescens FW300-N1B4

Align cystathionine gamma-lyase (EC 4.4.1.1) (characterized)
to candidate Pf1N1B4_4890 Cystathionine gamma-lyase (EC 4.4.1.1)

Query= BRENDA::Q5H4T8
         (397 letters)



>FitnessBrowser__pseudo1_N1B4:Pf1N1B4_4890
          Length = 393

 Score =  540 bits (1390), Expect = e-158
 Identities = 258/377 (68%), Positives = 309/377 (81%)

Query: 18  ATLAIHGGQSPDPSTGAVMPPIYATSTYAQSSPGEHQGFEYSRTHNPTRFAYERCVAALE 77
           AT  IH GQ+PDPSTGA+MPPIYA STY Q SPG H+GF+Y R+HNPTRFA ERCVA LE
Sbjct: 14  ATRVIHAGQTPDPSTGALMPPIYANSTYLQQSPGVHKGFDYGRSHNPTRFALERCVADLE 73

Query: 78  GGTRAFAFASGMAATSTVMELLDAGSHVVAMDDLYGGTFRLFERVRRRTAGLDFSFVDLT 137
           GGTRAFAFASG+AA + V+ELLDAG+H+V+ +DLYGGTFRLF++VRRR+AG  FSFVDLT
Sbjct: 74  GGTRAFAFASGLAAIANVLELLDAGAHIVSGNDLYGGTFRLFDKVRRRSAGHRFSFVDLT 133

Query: 138 DPAAFKAAIRADTKMVWIETPTNPMLKLVDIAAIAVIARKHGLLTVVDNTFASPMLQRPL 197
           D AAF+AA+  DT+MVW+ETP+NP+L L D+ A+A I R+ G++ V DNTFASP +QRPL
Sbjct: 134 DLAAFEAALEDDTRMVWVETPSNPLLSLTDLDAVARICRQRGIICVADNTFASPWIQRPL 193

Query: 198 SLGADLVVHSATKYLNGHSDMVGGIAVVGDNAELAEQMAFLQNSIGGVQGPFDSFLALRG 257
            LG D+V+HS TKYLNGHSD++GGIAVVG NAELAE++ FLQN++G + GPFD+FL LRG
Sbjct: 194 ELGFDIVLHSTTKYLNGHSDVIGGIAVVGQNAELAERLGFLQNAVGAIAGPFDAFLTLRG 253

Query: 258 LKTLPLRMRAHCENALALAQWLETHPAIEKVIYPGLASHPQHVLAKRQMSGFGGIVSIVL 317
           +KTL LRM  HC NAL LAQWLE  P + +V YPGL SHPQH LA+RQM GFGG++S+ L
Sbjct: 254 VKTLALRMERHCSNALELAQWLERQPQVARVYYPGLPSHPQHELARRQMRGFGGMISLDL 313

Query: 318 KGGFDAAKRFCEKTELFTLAESLGGVESLVNHPAVMTHASIPVARREQLGISDALVRLSV 377
                 AKRF E   +F LAESLGGVESL+ HPA+MTHASIPV  R QLGI DALVRLSV
Sbjct: 314 NSDLAGAKRFLESVRIFALAESLGGVESLIEHPAIMTHASIPVETRAQLGIGDALVRLSV 373

Query: 378 GIEDLGDLRGDLERALV 394
           G+ED+ DLR DL +AL+
Sbjct: 374 GVEDVEDLRADLAQALM 390


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: 558
Number of extensions: 23
Number of successful extensions: 1
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: 393
Length adjustment: 31
Effective length of query: 366
Effective length of database: 362
Effective search space:   132492
Effective search space used:   132492
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