GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metC in Pseudomonas fluorescens FW300-N2C3

Align cystathionine gamma-lyase (EC 4.4.1.1) (characterized)
to candidate AO356_15115 AO356_15115 cystathionine gamma-synthase

Query= BRENDA::Q5H4T8
         (397 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_15115
          Length = 417

 Score =  268 bits (684), Expect = 3e-76
 Identities = 159/383 (41%), Positives = 222/383 (57%), Gaps = 12/383 (3%)

Query: 19  TLAIHGGQSPDPSTGAVMPPIYATSTYAQS--------SPGEHQGFEYSRTHNPTRFAYE 70
           T A+ GG+       A   PI A++ Y           + G+  GF YSR  NPT    E
Sbjct: 17  TRAVWGGEQVRHPYNATQTPIVASAAYGYDDIDVWYDVALGKAPGFIYSRMSNPTVETLE 76

Query: 71  RCVAALEGGTRAFAFASGMAATSTVM-ELLDAGSHVVAMDDLYGGTFRLFERVRRRTAGL 129
             +  LE    A AF+SGMAA S+V+   L  G  VV+  D YGGT ++FE    RT G+
Sbjct: 77  AKIRELEMAESAVAFSSGMAAISSVLYTFLAHGDRVVSTKDSYGGTNKIFEEFLPRT-GV 135

Query: 130 DFSFVDLTDPAAFKAAIRADTKMVWIETPTNPMLKLVDIAAIAVIARKHGLLTVVDNTFA 189
             +  +  D    +  I    +++++ETPTNP LK++DI  +   A++ G + V DNTFA
Sbjct: 136 AVTLCETFDHDDIEREIAKGCQVLYLETPTNPTLKILDIPRLVAAAKRVGAVVVADNTFA 195

Query: 190 SPMLQRPLSLGADLVVHSATKYLNGHSDMVGGIAVVGDNAELAEQMAFLQNSIGGVQGPF 249
           +P+ Q PL+LG D+V+HSATK+L+GH D++GG+ V G  A +A+   + + + G    PF
Sbjct: 196 TPLNQSPLALGVDVVIHSATKFLSGHGDVLGGL-VCGREALMAKVRHYREIN-GASLDPF 253

Query: 250 DSFLALRGLKTLPLRMRAHCENALALAQWLETHPAIEKVIYPGLASHPQHVLAKRQMSGF 309
            ++L +RG+KTL LRMR    +A ALA++L T P +E V YPGL SHP H +A  QMSGF
Sbjct: 254 SAYLIIRGMKTLALRMRQQQHSARALAEFLCTEPLVESVNYPGLPSHPNHAVACAQMSGF 313

Query: 310 GGIVSIVLKGGFDAAKRFCEKTELFTLAESLGGVESLVNHPAVMTHASIPVARREQLGIS 369
           G IVS VL GG D  K    +      A +LG VE++       +H    +  R+ LGIS
Sbjct: 314 GAIVSFVLAGGMDTVKLLLPRLRFAHCAGNLGAVETIYGPARTTSHVENTLEERQALGIS 373

Query: 370 DALVRLSVGIEDLGDLRGDLERA 392
           + LVR+SVGIED  DL  DL++A
Sbjct: 374 EGLVRVSVGIEDTDDLLDDLKQA 396


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: 471
Number of extensions: 21
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: 397
Length of database: 417
Length adjustment: 31
Effective length of query: 366
Effective length of database: 386
Effective search space:   141276
Effective search space used:   141276
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