GapMind for Amino acid biosynthesis

 

Alignments for a candidate for metB in Methylocystis bryophila S285

Align cystathionine gamma-synthase (EC 2.5.1.48) (characterized)
to candidate WP_085773091.1 B1812_RS19675 cystathionine beta-lyase

Query= BRENDA::L0EK12
         (534 letters)



>NCBI__GCF_002117405.1:WP_085773091.1
          Length = 398

 Score =  198 bits (504), Expect = 3e-55
 Identities = 127/369 (34%), Positives = 190/369 (51%), Gaps = 13/369 (3%)

Query: 166 ITTPVVNTSAYFFKKTADLIDFKEKRQTSYEYGRYGNPTSTVLEEKISELEGAESTVLMA 225
           + TPV   S   F    D     E+ +  Y Y   G PT+  LEE  SEL GA +TVL  
Sbjct: 32  VNTPVYRGSTVLFPTAEDF----ERHRQPYTYATKGTPTTRGLEEAWSELSGATTTVLAP 87

Query: 226 SGMCASIVLLMALVPAGGHLVTTTDCYRKTRIFIETVLPKMGITTTVVDPADVGALESAL 285
           SG+ A  + LM    AG HL+ T   Y  TRIF + VL + G+ T   DP  +GA   AL
Sbjct: 88  SGLAAIALALMTATKAGDHLLVTDSAYGPTRIFCDGVLKRFGVETQYYDPR-LGAGVGAL 146

Query: 286 EQNNVSLFFTESPTNPFLRCVDIKLVSELCHKHGALLCIDGTFATPLNQKALALGADLIM 345
            + N S    ESP +  +   D+  ++      GA + +D T+ATPL       G D+ +
Sbjct: 147 MRENTSAILAESPGSLTMEVQDVPAIAAAAAARGACVILDNTWATPLFFPPFERGVDINV 206

Query: 346 HSCTKYMGGHHDVLGGCISGSDKLISQIRILHHILGGALNPNAAYLFIRGMKTLHLRVQQ 405
            + TKY+ GH D+L G +S + K  +++R            + A+L +RG++T+ LR+++
Sbjct: 207 EAGTKYLSGHADLLLGLVSANAKWATRLRNSFDAFAMVPGGDDAFLALRGLRTMELRLRE 266

Query: 406 QNSTGMRMAKLLEAHPKVKRVYYPGLPSHPEHELAMRQMTGFGGVVSFEIDGDLTTTI-K 464
           Q   G+ +A+ LE   +V R+ +P LP+HP+H L  R  +G  GV S  ++      +  
Sbjct: 267 QQRAGLEIAQWLEGRSEVLRLLHPALPAHPDHALWKRDFSGAAGVFSVVLNPAPKPCVDA 326

Query: 465 FVDSLKIPYIAASFGGCESIVDQPAILSYWDLPASERAK-YKIYDNLVRFSFGVEDFEDL 523
           F+++L +  I  S+GG ES+V        +D   S  A  +      +RFS G+ED EDL
Sbjct: 327 FLNALTLFGIGYSWGGYESLVIP------FDCARSRTATCFAPEGPCLRFSIGLEDVEDL 380

Query: 524 KADILQALE 532
           KAD+  A E
Sbjct: 381 KADLAAAFE 389


Lambda     K      H
   0.319    0.134    0.393 

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: 455
Number of extensions: 20
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: 534
Length of database: 398
Length adjustment: 33
Effective length of query: 501
Effective length of database: 365
Effective search space:   182865
Effective search space used:   182865
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: 51 (24.3 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.

Links

Downloads

Related tools

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