Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_038806127.1 HK29_RS05075 NADP-dependent glyceraldehyde-3-phosphate dehydrogenase
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000382825.1:WP_038806127.1 Length = 474 Score = 228 bits (582), Expect = 3e-64 Identities = 156/476 (32%), Positives = 250/476 (52%), Gaps = 22/476 (4%) Query: 24 INGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANRAVENARATFNSGVWSQLAPAKR 83 +NG + S + SP++ L V + A+ + A++ ARA + W LAP +R Sbjct: 8 VNGNWKS--SEKEITIYSPINQEKLGTVPAMSQAEVDEAMKAARAALPA--WRDLAPVER 63 Query: 84 KAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDIPGAAQAIHWTAEAIDKVYDEVA 143 A L + AD+L ++ E++ + ++ K I + ++ A I + AE ++ + Sbjct: 64 AAYLHKTADILERDKEKIGTILAKEVAKGIKAAIG-EVVRTADLIRFAAEEGLRITGQAM 122 Query: 144 P------TPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPALATGNSVVLKPSEKSP 197 ++L +V REPVGVV AI P+N+P+ ++ K+ PAL GN V+ KP + Sbjct: 123 EGGGFEAASKNKLAVVRREPVGVVLAIAPFNYPVNLSGSKIAPALIAGNVVMFKPPTQGS 182 Query: 198 LTAIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMVYAG 257 ++ + +A+ EAGIPAGV N + G G +G + H +V+ + FTGST I +++ AG Sbjct: 183 ISGLLLAKAFDEAGIPAGVFNTITGRGSEIGDYIIEHKEVNFINFTGSTPIGERIGRLAG 242 Query: 258 ESNMKRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEVCTAGSRLLVERSIKDK 317 M+ I LE GGK IV DA DL+ AA+ G+ CTA R+LV S+ D+ Sbjct: 243 ---MRPIMLELGGKDAAIVLEDA-DLEHAAKQIVGGAFSYSGQRCTAIKRVLVVESVADR 298 Query: 318 FLPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGHKDGAKLLAGGKRTLEE 377 ++ + G+P D + +VD + + I+ + GAK L+ KR Sbjct: 299 LAELLQAEVAKLTVGDPFD-NADITPVVDNASADFIWGLIQDAQEKGAKALSPIKRE--- 354 Query: 378 TGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAIANDTPYGLAAGIWTSD 437 G + P +FD VT M++A EE+FGPVL +I A EAVAIAN++ +GL + ++T+D Sbjct: 355 --GNLIWPGLFDYVTRDMKLAWEELFGPVLPIIRVADANEAVAIANESEFGLQSSVFTND 412 Query: 438 ISKAHKTARAVRAGSVWV-NQYDGGDMTAPFGGFKQSGNGRDKSLHALEKYTELKA 492 KA + A + G+V + N+ G PF G K SG G +++E T +K+ Sbjct: 413 FKKAFEIAEKLEVGTVHINNKTQRGPDNFPFLGVKGSGAGVQGIKYSIEAMTNVKS 468 Lambda K H 0.316 0.132 0.390 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: 564 Number of extensions: 36 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: 497 Length of database: 474 Length adjustment: 34 Effective length of query: 463 Effective length of database: 440 Effective search space: 203720 Effective search space used: 203720 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 Sep 24 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:
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