GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metC in Sinorhizobium meliloti 1021

Align cystathionine gamma-lyase (EC 4.4.1.1) (characterized)
to candidate SMc02217 SMc02217 O-succinylhomoserine sulfhydrylase

Query= BRENDA::Q5H4T8
         (397 letters)



>FitnessBrowser__Smeli:SMc02217
          Length = 394

 Score =  240 bits (613), Expect = 5e-68
 Identities = 146/389 (37%), Positives = 219/389 (56%), Gaps = 12/389 (3%)

Query: 18  ATLAIHGGQSPDPSTGAVMPPIYATSTYAQSSP--------GEHQGFEYSRTHNPTRFAY 69
           AT  +HGG       G     I+ T  +   S         GE  GF Y+R  +PT   +
Sbjct: 8   ATQLVHGGTLRS-QYGETSEAIFLTQGFVYDSSEAAEARFKGETDGFIYARYGSPTNDMF 66

Query: 70  ERCVAALEGGTRAFAFASGMAATST-VMELLDAGSHVVAMDDLYGGTFRLFERVRRRTAG 128
           E+ +  LEG   A A ASGMAA S  ++  + AG H+VA   L+G    + E +  +  G
Sbjct: 67  EKRMCMLEGAEDARATASGMAAVSAAILCQVKAGDHIVAARALFGSCRWVVETLAPKY-G 125

Query: 129 LDFSFVDLTDPAAFKAAIRADTKMVWIETPTNPMLKLVDIAAIAVIARKHGLLTVVDNTF 188
           ++ + VD  D   ++ A+R +TK+ ++E+PTNP L+++DIA +A +A + G   VVDN F
Sbjct: 126 VECTLVDGRDLKNWEDAVRPNTKVFFLESPTNPTLEVIDIAGVARLADQIGAKVVVDNVF 185

Query: 189 ASPMLQRPLSLGADLVVHSATKYLNGHSDMVGGIAVVGDNAELAEQMAFLQNSIGGVQGP 248
           A+P+ Q+PL LGA +VV+SATK+++G    +GG+ V+ D   + E +       G    P
Sbjct: 186 ATPLFQKPLELGAHVVVYSATKHIDGQGRCLGGV-VLSDKQWVDENLHDYFRHTGPAMSP 244

Query: 249 FDSFLALRGLKTLPLRMRAHCENALALAQWLETHPAIEKVIYPGLASHPQHVLAKRQMSG 308
           F+++  L+G++TLPLR++   E+A  +A +L   P + +VIYPG   HPQ  +  +QMSG
Sbjct: 245 FNAWTLLKGIETLPLRVKQQTESARRVADFLAEQPQVARVIYPGRKDHPQADVIAKQMSG 304

Query: 309 FGGIVSIVLKGGFDAAKRFCEKTELFTLAESLGGVESLVNHPAVMTHASIPVARREQLGI 368
              +V+  LKGG +AA       E+  ++ +LG  +SL+ HPA  TH ++    R +LGI
Sbjct: 305 GSTLVAFELKGGKEAAFALQNALEIIRISNNLGDSKSLITHPATTTHKNLTDEARAELGI 364

Query: 369 SDALVRLSVGIEDLGDLRGDLERALVNQN 397
           S   VR S GIED  DL  D  RAL   N
Sbjct: 365 SAGTVRFSAGIEDSEDLIEDFARALKGVN 393


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: 397
Number of extensions: 13
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: 394
Length adjustment: 31
Effective length of query: 366
Effective length of database: 363
Effective search space:   132858
Effective search space used:   132858
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