GapMind for Amino acid biosynthesis

 

Alignments for a candidate for CGL in Methanobacterium lacus AL-21

Align cystathionine gamma-lyase (EC 4.4.1.1) (characterized)
to candidate WP_013644861.1 METBO_RS06350 cystathionine gamma-synthase

Query= metacyc::HP_RS00540-MONOMER
         (380 letters)



>NCBI__GCF_000191585.1:WP_013644861.1
          Length = 377

 Score =  385 bits (990), Expect = e-112
 Identities = 187/374 (50%), Positives = 255/374 (68%), Gaps = 2/374 (0%)

Query: 1   MRMQTKLIHGGISEDATTGAVSVPIYQTSTYRQDAIGRHKGYEYSRSGNPTRFALEELIA 60
           M+  T+ IH G   D  TGA+S  I QTST+  D   +   Y+YSR+GNPTR ALEE IA
Sbjct: 1   MKFSTRSIHAGRKPDPITGAISPTICQTSTFTFDEFNKPGDYDYSRTGNPTRSALEEAIA 60

Query: 61  DLEGGVKGFAFASGLAGIHAVFSLLQSGDHVLLGDDVYGGTFRLFNQVLVKNGLSCTIID 120
           +LEGG  GF F+SG+A +     LL+SGDH ++G+D+YGGT RLF++++ K G+  T I 
Sbjct: 61  NLEGGNAGFCFSSGMAAVTTAIHLLKSGDHAVVGEDIYGGTHRLFSEIMTKYGIDFTFIR 120

Query: 121 TSDISQIKKAIKPNTKALYLETPSNPLLKITDLAQCASVAKDHGLLTIVDNTFATPYYQN 180
                +++ AIKPNTK +++ETPSNPLL ITDL+  + +AK+  +LT+ DNTF +PY+  
Sbjct: 121 MDSEEKLEAAIKPNTKMIWIETPSNPLLNITDLSMVSKIAKEKQILTVADNTFPSPYFLR 180

Query: 181 PLLLGADIVAHSGTKYLGGHSDVVAGLVTTNNEALAQEIAFFQNAIGGVLGPQDSWLLQR 240
           P+  G D+V HS TKY+ GHSDV+ G + T  E LA+++ F  N +G    P DSWL+ R
Sbjct: 181 PIEYGIDLVLHSTTKYINGHSDVIGGAIVTTTEELAKDVHFLLNGMGTNAAPFDSWLILR 240

Query: 241 GIKTLGLRMEAHQKNALCVAEFLEKHPKVERVYYPGLPTHPNYELAKKQMRGFSGMLSFT 300
           G+KTL LRME H  NA+ VAE+L  HPKV  V+YPGL +HP + +AK QM G+ G++SF 
Sbjct: 241 GLKTLPLRMEKHASNAIAVAEYLLDHPKVSEVFYPGLESHPGHSIAKNQMDGYGGVVSFK 300

Query: 301 LKNDSEAVAFVESLKLFILGESLGGVESLVGIPAFMTHACIPKTQREAAGIRDGLVRLSV 360
           LK D     F+ESL++F L ESLGG +SLV   A M+HA +    R+ AGI D ++RLS+
Sbjct: 301 LKTD--VPKFIESLEIFHLAESLGGADSLVEHAATMSHASMSPDARKQAGISDDIIRLSI 358

Query: 361 GIEHEQDLLEDLEQ 374
           G+E   DL+EDL +
Sbjct: 359 GLEDNDDLIEDLSK 372


Lambda     K      H
   0.319    0.137    0.394 

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: 417
Number of extensions: 22
Number of successful extensions: 2
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: 380
Length of database: 377
Length adjustment: 30
Effective length of query: 350
Effective length of database: 347
Effective search space:   121450
Effective search space used:   121450
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 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 10 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