GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metC in Phaeobacter inhibens BS107

Align cystathionine gamma-lyase (EC 4.4.1.1) (characterized)
to candidate GFF1638 PGA1_c16600 methionine gamma-lyase MdeA

Query= BRENDA::Q5H4T8
         (397 letters)



>FitnessBrowser__Phaeo:GFF1638
          Length = 401

 Score =  308 bits (790), Expect = 1e-88
 Identities = 174/392 (44%), Positives = 236/392 (60%), Gaps = 12/392 (3%)

Query: 16  SLATLAIHGGQSPDPSTGAVMPPIYATSTYAQSSP--------GEHQGFEYSRTHNPTRF 67
           S +T AIH G       G++ PP+Y TST+   S         GE +G  YSR  NPT  
Sbjct: 7   SFSTRAIHHGYDTQSQQGSLNPPLYLTSTFTFDSAEAGGEMFTGEREGHFYSRISNPTLD 66

Query: 68  AYERCVAALEGGTRAFAFASGMAA-TSTVMELLDAGSHVVAMDDLYGGTFRLFERVRRRT 126
             E+ +A LEGG    A ASGM A TST+   L AG  ++    LYG TF        R 
Sbjct: 67  HLEQRIANLEGGEAGLATASGMGAITSTLWSFLAAGDEIILDKTLYGCTFSFMTHGLPRF 126

Query: 127 AGLDFSFVDLTDPAAFKAAIRADTKMVWIETPTNPMLKLVDIAAIAVIARKHGLLTVVDN 186
            G+    VD+TDP     AI   TK+V+ ETP NP  +L+DIAAI+ IA K G   VVDN
Sbjct: 127 -GVKVRLVDMTDPTNLAEAISPKTKLVYFETPANPNNRLIDIAAISEIAHKAGAKVVVDN 185

Query: 187 TFASPMLQRPLSLGADLVVHSATKYLNGHSDMVGGIAVVGDNAELAE-QMAFLQNSIGGV 245
           TFA+P+L RP+ LGAD+VVHSATK+++GH D++ G+ VVG   E+ + ++  L++  G V
Sbjct: 186 TFATPVLTRPIELGADIVVHSATKFISGHGDVIAGL-VVGSKEEITQIRLVGLKDMTGAV 244

Query: 246 QGPFDSFLALRGLKTLPLRMRAHCENALALAQWLETHPAIEKVIYPGLASHPQHVLAKRQ 305
             PF + L +RGLKTL LRM  HC++AL +A+ L+ HPA+E+V YPGL    Q  LA+RQ
Sbjct: 245 MSPFSAMLLMRGLKTLELRMERHCKSALKVAEALQAHPAVERVYYPGLDDFAQGDLARRQ 304

Query: 306 MSGFGGIVSIVLKGGFDAAKRFCEKTELFTLAESLGGVESLVNHPAVMTHASIPVARREQ 365
           MSGFGG++   + GG         +  +   A SLG  E+L+ HPA MTH++     R +
Sbjct: 305 MSGFGGMIPFEVVGGKAGGIAMMNRLAMIQRAVSLGDAETLIQHPASMTHSTYTPEERAE 364

Query: 366 LGISDALVRLSVGIEDLGDLRGDLERALVNQN 397
            GI++ LVR+SVG+E + D+  DL +AL + N
Sbjct: 365 HGIAEGLVRMSVGLEGVDDIIDDLMQALSSHN 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: 481
Number of extensions: 23
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: 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