Align phosphopentomutase (EC 5.4.2.7) (characterized)
to candidate Pf6N2E2_3357 Phosphoglucosamine mutase (EC 5.4.2.10)
Query= BRENDA::Q6I7B6 (450 letters) >FitnessBrowser__pseudo6_N2E2:Pf6N2E2_3357 Length = 445 Score = 135 bits (339), Expect = 3e-36 Identities = 128/449 (28%), Positives = 210/449 (46%), Gaps = 50/449 (11%) Query: 2 RLFGTAGIRGTLWE-KVTPELAMKVGMAVGTY--KSG--KALVGRDGRTSSVMLKNAMIS 56 + FGT GIRG + E +TP+ +K+G A G K G K LVG+D R S M ++A+ + Sbjct: 4 KYFGTDGIRGRVGEYPITPDFMLKLGWAAGMAFRKMGACKVLVGKDTRISGYMFESALEA 63 Query: 57 GLLSTGMEVLDADLIPTPALAWGTRKL-ADAGVMITASHNPPTDNGVKVFNGDGTEFYVE 115 GL S G +V+ +PTPA+A+ TR A AG++I+ASHNP DNG+K F+G GT+ + Sbjct: 64 GLTSAGADVMLLGPMPTPAIAYLTRTFQAQAGIVISASHNPHDDNGIKFFSGQGTKLPDD 123 Query: 116 QERGLEE-------IIFSGNFRKARWDEIKPVRNVEVIPDYINAVLDFVGHETNLKVLYD 168 E +EE ++ S K R +E + F G LK++ D Sbjct: 124 IELMIEELLDTPMTVVESSKIGKVSRINDASGRYIEFCKGSVPTGTSFSG----LKIVVD 179 Query: 169 GANGAGSLVAPYLLREMGAKVLSVNAHVDGHFPGRKPEPRYENIAYLGKLVRELGVDLAI 228 A+GA VAP + RE+GA+V+ ++A +G + L + DL I Sbjct: 180 CAHGATYKVAPSVFRELGAEVVVLSAQPNGLNINHNCGSTHTEALQAAVLAEQ--ADLGI 237 Query: 229 AQDGDADRIAVFDEKGNYVDEDTVIALFAKLYVEEHGGGT----VVVSIDTGSRIDAVVE 284 A DGD DR+ + D G VD D ++ + A+ + HG G VV ++ + ++ + Sbjct: 238 AFDGDGDRVLMVDHTGTVVDGDELLFIIAR---DLHGRGKLQGGVVGTLMSNLGLELALA 294 Query: 285 RAGGRVVRIPLGQPH---DGIKRYKAIFAAEPWKLV---HPKFGPWIDPFVTMGLLIKLI 338 VR +G + + ++R I +V H G I + + + +K Sbjct: 295 DLDIPFVRANVGDRYVISELLERNWVIGGENSGHIVCFDHTTTGDAIIAALQVLMALKAR 354 Query: 339 DENGPLS-ELVKEIPTYYLKKANVLCPDEYKAEVVRRAAEEVERKLSSEIKEVLTISGFR 397 +E S + +++ P + + + V++A+E V + ++ + Sbjct: 355 NEGLAQSRQALRKCPQVLINVRFGGGVNPLEHAKVKQASEHVTQAMAGRGR--------- 405 Query: 398 IALNDGSWILIRPSGTEPKIRVVAEAPTE 426 +L+R SGTEP +RV+ E E Sbjct: 406 --------VLLRKSGTEPLVRVMVEGEDE 426 Lambda K H 0.318 0.138 0.402 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: 466 Number of extensions: 27 Number of successful extensions: 5 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 450 Length of database: 445 Length adjustment: 33 Effective length of query: 417 Effective length of database: 412 Effective search space: 171804 Effective search space used: 171804 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: 51 (24.3 bits)
This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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