Align glycine hydroxymethyltransferase (EC 2.1.2.1) (characterized)
to candidate WP_057507786.1 ABB28_RS06065 serine hydroxymethyltransferase
Query= BRENDA::R9YJZ9 (417 letters) >NCBI__GCF_001431535.1:WP_057507786.1 Length = 417 Score = 626 bits (1614), Expect = 0.0 Identities = 297/417 (71%), Positives = 352/417 (84%) Query: 1 MLKKAMNIADYDPELFKAIEDETRRQEEHIELIASENYTSPRVMEAQGSQLTNKYAEGYP 60 M + + I YDPEL KAI DE++RQE+H+ELIASENY SP VMEAQGSQLTNKYAEGYP Sbjct: 1 MFPRDVRIESYDPELAKAIADESQRQEDHVELIASENYASPMVMEAQGSQLTNKYAEGYP 60 Query: 61 GKRYYGGCEYVDVVETLAIERAKQLFGATYANVQPHSGSQANSAVYMALLQPGDTVLGMN 120 GKRYYGGCEYVD+ E LAI+R KQL+GA YANVQPHSGSQAN AVY ALLQ GDT+LGM+ Sbjct: 61 GKRYYGGCEYVDIAEQLAIDRLKQLYGADYANVQPHSGSQANQAVYFALLQAGDTILGMS 120 Query: 121 LAHGGHLTHGSPVNFSGKLYNIIPYGIDESGKIDYSELETLALEHKPKMIIGGFSAYSGI 180 LAHGGHLTHG+ VN SGKL+N + YG+++ G IDY E+E LA+EHKPKM++ GFSAYS + Sbjct: 121 LAHGGHLTHGAKVNASGKLFNAVQYGVNDQGLIDYDEVERLAVEHKPKMVVAGFSAYSQV 180 Query: 181 VDWAKLREIADKIGAYLFVDMAHVAGLIAAGVYPNPVPHAHVVTSTTHKTLAGPRGGVIL 240 VDWA+ R IADK+GAYLFVDMAHVAGL+AAGVYP+P+ HAHVVTSTTHKTL GPRGG+I+ Sbjct: 181 VDWARFRAIADKVGAYLFVDMAHVAGLVAAGVYPSPLEHAHVVTSTTHKTLRGPRGGIII 240 Query: 241 SAADDEDLYKKLNSAVFPGGQGGPLMHVIAGKAVAFKEALEPEFKTYQQQVVNNAKAMVE 300 + E+L KKL S VFPG QGGPLMHVIA KAVAFKEALEP+F YQQQVV NA+AM + Sbjct: 241 AKGASEELVKKLQSIVFPGIQGGPLMHVIAAKAVAFKEALEPDFTRYQQQVVKNAQAMAK 300 Query: 301 VFLERGYKIVSGGTDNHLMLVDLIGRELTGKEADAALGRANITVNKNSVPNDPRSPFVTS 360 + RGYKIVSGGT+NHLMLVD+IG++++GK+A+AALG+A+ITVNKNSVPNDPRSPFVTS Sbjct: 301 TLIARGYKIVSGGTENHLMLVDMIGKDVSGKDAEAALGKAHITVNKNSVPNDPRSPFVTS 360 Query: 361 GVRIGTPAITRRGFKEAEARELTGWICDVLDNAHDDAVIERVKSQVLELCARFPVYG 417 G+R+GTPA+T RG+ E + +L WI DVLD D+AVI RV+ V C ++PVYG Sbjct: 361 GLRLGTPAVTTRGYGEQDCVDLANWIADVLDAPADEAVIARVRDAVSAQCRKYPVYG 417 Lambda K H 0.316 0.135 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: 663 Number of extensions: 24 Number of successful extensions: 1 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: 417 Length of database: 417 Length adjustment: 31 Effective length of query: 386 Effective length of database: 386 Effective search space: 148996 Effective search space used: 148996 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.
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:
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