Align triose-phosphate isomerase (EC 5.3.1.1) (characterized)
to candidate WP_011373368.1 SUDEN_RS09125 phosphoglycerate kinase
Query= BRENDA::P36204 (654 letters) >NCBI__GCF_000012965.1:WP_011373368.1 Length = 399 Score = 402 bits (1033), Expect = e-116 Identities = 202/402 (50%), Positives = 282/402 (70%), Gaps = 8/402 (1%) Query: 1 MEKMTIRDVDLKGKRVIMRVDFNVPVKD-GVVQDDTRIRAALPTIKYALEQGAKVILLSH 59 ME + I+++DL GK+V +R DFNVP+ + G + DD RIR+A+ TI Y L+Q VIL SH Sbjct: 1 MELLNIKNLDLAGKKVFIRCDFNVPMDEFGNISDDRRIRSAVSTINYCLDQECAVILASH 60 Query: 60 LGRPKGEPSPEFSLAPVAKRLSELLGKEVKFVPAVVGDEVKKAVEELKEGEVLLLENTRF 119 LGRP+GE ++SL P+A+R+ LL +EV VVG++ K ELK G+VL+LEN R+ Sbjct: 61 LGRPEGEVVDKYSLIPIARRIQHLLRREVDLASDVVGEDALKRASELKSGQVLMLENLRY 120 Query: 120 HPGETKNDPELAKFWASLADIHVNDAFGTAHRAHASNVGIAQFIP---SVAGFLMEKEIK 176 GETKND EL+K AS+AD ++NDAFG +HRAHAS GI F AGFL++KEI Sbjct: 121 EAGETKNDKELSKKLASMADFYINDAFGVSHRAHASVEGITHFFDDKHKAAGFLLQKEID 180 Query: 177 FLSKVTYNPEKPYVVVLGGAKVSDKIGVITNLMEKADRILIGGAMMFTFLKALGKEVGSS 236 FL K+ NP +P+ ++GG+KVS K+ + NL+ + D++LIGG M FTFLK LG ++G+S Sbjct: 181 FLGKIIQNPVRPFAAIVGGSKVSGKLEALINLLPRVDKVLIGGGMAFTFLKKLGYDIGAS 240 Query: 237 RVEEDKIDLAKELLEKAKEKGVEIVLPVDAVIAQKIEPGVEKKVVRIDDGIPEGWMGLDI 296 VE+D ++ A ++++AK+ GV+ LPVD V+A K K+V + IP WMGLDI Sbjct: 241 LVEDDLLEEAGRIMDEAKKLGVKFYLPVDVVVADKFSEDAISKIVSYQE-IPPLWMGLDI 299 Query: 297 GPETIELFKQKLSDAKTVVWNGPMGVFEIDDFAEGTKQVALAIAALTEKGAITVVGGGDS 356 GP T+ L+ + LSD +TV+WNGPMGV+E+D FA G+ ++A +A + A T+VGGGD+ Sbjct: 300 GPATVRLYGEVLSDVQTVLWNGPMGVYEMDKFARGSNKIAHFVA---DSYATTIVGGGDT 356 Query: 357 AAAVNKFGLEDKFSHVSTGGGASLEFLEGKELPGIASIADKK 398 A V + G++D+ + +STGGGASLE LEGK LPG+AS+ KK Sbjct: 357 ADLVQRIGVDDEMTFISTGGGASLELLEGKILPGVASLIRKK 398 Lambda K H 0.317 0.137 0.386 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: 700 Number of extensions: 43 Number of successful extensions: 5 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: 654 Length of database: 399 Length adjustment: 34 Effective length of query: 620 Effective length of database: 365 Effective search space: 226300 Effective search space used: 226300 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: 52 (24.6 bits)
This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 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