GapMind for Amino acid biosynthesis

 

Alignments for a candidate for CGL in Thauera aminoaromatica S2

Align cystathionine gamma-lyase (EC 4.4.1.1) (characterized)
to candidate WP_004322211.1 C665_RS15845 O-succinylhomoserine sulfhydrylase

Query= BRENDA::Q5H4T8
         (397 letters)



>NCBI__GCF_000310185.1:WP_004322211.1
          Length = 394

 Score =  295 bits (754), Expect = 2e-84
 Identities = 164/364 (45%), Positives = 228/364 (62%), Gaps = 12/364 (3%)

Query: 39  IYATSTYAQSSP--------GEHQGFEYSRTHNPTRFAYERCVAALEGGTRAFAFASGMA 90
           +Y TS++   S         GE +G+ Y+R  NPT  A +  +AALEGG    A ASGM+
Sbjct: 32  MYLTSSFVFDSAAQAAACFSGEEEGYVYARFSNPTVTAMQNRLAALEGGEACIATASGMS 91

Query: 91  AT-STVMELLDAGSHVVAMDDLYGGTFRLFERVRRRTAGLDFSFVDLTDPAAFKAAIRAD 149
           A  S  M  + AG HVVA + L+G T +LF  +  +  G+  SFV  T+  A++AA+   
Sbjct: 92  AILSLAMATMQAGDHVVASNGLFGATQQLFGGILSKF-GIATSFVPATELDAWRAAVTPR 150

Query: 150 TKMVWIETPTNPMLKLVDIAAIAVIARKHGLLTVVDNTFASPMLQRPLSLGADLVVHSAT 209
           T++ + ETP+NP+ +++DIA +A IAR  G++  VDN F +P LQRPL LGAD+VVHSAT
Sbjct: 151 TRLFFTETPSNPLTEVIDIAGVAAIARAAGVIFAVDNCFCTPALQRPLELGADVVVHSAT 210

Query: 210 KYLNGHSDMVGGIAVVGDNAELAEQMAFLQNSIGGVQGPFDSFLALRGLKTLPLRMRAHC 269
           KYL+G   ++GG AVVG  A   E   FL+ + G    PF++++ L+GL+TL +RM A  
Sbjct: 211 KYLDGQGRVLGG-AVVGSKAITDEVFKFLRTA-GPTLSPFNAWVILKGLETLRIRMEAQS 268

Query: 270 ENALALAQWLETHPAIEKVIYPGLASHPQHVLAKRQMSGFGGIVSIVLKGGFDAAKRFCE 329
            +AL LA+WLE  P + +V YPGL SHPQHVLA RQ    G IVS  +KGG +AA +  +
Sbjct: 269 ASALELARWLEAQPGVARVYYPGLESHPQHVLAMRQQKSGGAIVSFDVKGGREAAWKVVD 328

Query: 330 KTELFTLAESLGGVESLVNHPAVMTHASIPVARREQLGISDALVRLSVGIEDLGDLRGDL 389
            T L ++  +LG  +S + HPA  TH  I    R   GI D L+R++VG+ED+ DL+ DL
Sbjct: 329 ATRLISITANLGDTKSTITHPATTTHGRISAEARATAGIGDGLLRIAVGLEDVDDLKADL 388

Query: 390 ERAL 393
            R L
Sbjct: 389 ARGL 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: 448
Number of extensions: 18
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 Jul 25 2024. The underlying query database was built on Jul 25 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