Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 20 |
NetGPI | no | yes: 0, no: 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:0005759 | mitochondrial matrix | 5 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
Related structures:
AlphaFold database: A4HMH9
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006979 | response to oxidative stress | 3 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016485 | protein processing | 5 | 1 |
GO:0016540 | protein autoprocessing | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051604 | protein maturation | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0016787 | hydrolase activity | 2 | 3 |
GO:0004175 | endopeptidase activity | 4 | 1 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 1 |
GO:0008233 | peptidase activity | 3 | 1 |
GO:0008234 | cysteine-type peptidase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.145 |
CLV_NRD_NRD_1 | 232 | 234 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.468 |
CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.386 |
CLV_PCSK_PC1ET2_1 | 28 | 30 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.218 |
DEG_APCC_DBOX_1 | 85 | 93 | PF00400 | 0.271 |
DOC_CDC14_PxL_1 | 14 | 22 | PF14671 | 0.279 |
DOC_CYCLIN_yCln2_LP_2 | 185 | 191 | PF00134 | 0.357 |
DOC_CYCLIN_yCln2_LP_2 | 208 | 214 | PF00134 | 0.248 |
DOC_CYCLIN_yCln2_LP_2 | 312 | 318 | PF00134 | 0.370 |
DOC_MAPK_gen_1 | 28 | 35 | PF00069 | 0.276 |
DOC_MAPK_gen_1 | 294 | 301 | PF00069 | 0.298 |
DOC_MAPK_gen_1 | 61 | 69 | PF00069 | 0.279 |
DOC_MAPK_MEF2A_6 | 28 | 35 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 61 | 69 | PF00069 | 0.281 |
DOC_MAPK_RevD_3 | 14 | 29 | PF00069 | 0.446 |
DOC_PP2B_LxvP_1 | 185 | 188 | PF13499 | 0.407 |
DOC_PP2B_LxvP_1 | 208 | 211 | PF13499 | 0.248 |
DOC_PP2B_LxvP_1 | 395 | 398 | PF13499 | 0.532 |
DOC_PP4_MxPP_1 | 348 | 351 | PF00568 | 0.646 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.591 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.529 |
LIG_14-3-3_CanoR_1 | 373 | 379 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 392 | 396 | PF00244 | 0.734 |
LIG_14-3-3_CanoR_1 | 40 | 46 | PF00244 | 0.512 |
LIG_Actin_WH2_2 | 121 | 137 | PF00022 | 0.329 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.597 |
LIG_Clathr_ClatBox_1 | 165 | 169 | PF01394 | 0.316 |
LIG_eIF4E_1 | 313 | 319 | PF01652 | 0.401 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.407 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.254 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.761 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.247 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.338 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.250 |
LIG_LIR_Apic_2 | 213 | 217 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 179 | 190 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 209 | 219 | PF02991 | 0.248 |
LIG_LIR_Gen_1 | 271 | 280 | PF02991 | 0.258 |
LIG_LIR_Gen_1 | 281 | 287 | PF02991 | 0.237 |
LIG_LIR_Gen_1 | 428 | 434 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 108 | 114 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 138 | 144 | PF02991 | 0.222 |
LIG_LIR_Nem_3 | 179 | 185 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 209 | 215 | PF02991 | 0.227 |
LIG_LIR_Nem_3 | 271 | 275 | PF02991 | 0.243 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.222 |
LIG_LIR_Nem_3 | 311 | 316 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 317 | 322 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 428 | 432 | PF02991 | 0.721 |
LIG_NRBOX | 282 | 288 | PF00104 | 0.378 |
LIG_PCNA_yPIPBox_3 | 325 | 339 | PF02747 | 0.262 |
LIG_Pex14_1 | 374 | 378 | PF04695 | 0.608 |
LIG_SH2_CRK | 357 | 361 | PF00017 | 0.518 |
LIG_SH2_CRK | 51 | 55 | PF00017 | 0.415 |
LIG_SH2_GRB2like | 236 | 239 | PF00017 | 0.329 |
LIG_SH2_GRB2like | 282 | 285 | PF00017 | 0.407 |
LIG_SH2_NCK_1 | 357 | 361 | PF00017 | 0.421 |
LIG_SH2_NCK_1 | 405 | 409 | PF00017 | 0.648 |
LIG_SH2_PTP2 | 214 | 217 | PF00017 | 0.407 |
LIG_SH2_SRC | 282 | 285 | PF00017 | 0.316 |
LIG_SH2_SRC | 357 | 360 | PF00017 | 0.610 |
LIG_SH2_STAP1 | 161 | 165 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 427 | 430 | PF00017 | 0.729 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.262 |
LIG_SH3_2 | 47 | 52 | PF14604 | 0.411 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.333 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.357 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.322 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.298 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.636 |
LIG_SH3_3 | 395 | 401 | PF00018 | 0.685 |
LIG_SH3_3 | 404 | 410 | PF00018 | 0.698 |
LIG_SH3_3 | 413 | 419 | PF00018 | 0.650 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.353 |
LIG_SUMO_SIM_anti_2 | 3 | 9 | PF11976 | 0.459 |
LIG_TRAF2_1 | 289 | 292 | PF00917 | 0.407 |
LIG_UBA3_1 | 165 | 172 | PF00899 | 0.402 |
LIG_WRPW_2 | 313 | 316 | PF00400 | 0.435 |
LIG_WW_3 | 29 | 33 | PF00397 | 0.316 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.348 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.667 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.372 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.250 |
MOD_Cter_Amidation | 37 | 40 | PF01082 | 0.391 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.227 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.186 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.226 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.227 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.156 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.310 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.246 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.225 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.380 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.358 |
MOD_LATS_1 | 170 | 176 | PF00433 | 0.402 |
MOD_N-GLC_1 | 172 | 177 | PF02516 | 0.405 |
MOD_N-GLC_1 | 234 | 239 | PF02516 | 0.265 |
MOD_N-GLC_1 | 324 | 329 | PF02516 | 0.411 |
MOD_N-GLC_1 | 69 | 74 | PF02516 | 0.316 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.316 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.210 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.281 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.241 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.243 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.567 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.463 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.242 |
MOD_NEK2_2 | 23 | 28 | PF00069 | 0.409 |
MOD_PIKK_1 | 151 | 157 | PF00454 | 0.202 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.750 |
MOD_PK_1 | 172 | 178 | PF00069 | 0.402 |
MOD_PKA_2 | 151 | 157 | PF00069 | 0.356 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.222 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.554 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.538 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.411 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.567 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.366 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.232 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.428 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.529 |
TRG_DiLeu_BaEn_1 | 101 | 106 | PF01217 | 0.234 |
TRG_DiLeu_BaLyEn_6 | 37 | 42 | PF01217 | 0.371 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.252 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.473 |
TRG_ER_diArg_1 | 231 | 233 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 39 | 41 | PF00400 | 0.474 |
TRG_NLS_MonoExtC_3 | 293 | 298 | PF00514 | 0.407 |
TRG_NLS_MonoExtN_4 | 294 | 299 | PF00514 | 0.378 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HW49 | Leptomonas seymouri | 51% | 95% |
A0A0N1P9F5 | Leptomonas seymouri | 45% | 100% |
A0A0N1PDW0 | Leptomonas seymouri | 79% | 100% |
A0A0S4J2H4 | Bodo saltans | 54% | 95% |
A0A1X0NMB0 | Trypanosomatidae | 50% | 100% |
A0A1X0NMU0 | Trypanosomatidae | 51% | 100% |
A0A1X0P5R0 | Trypanosomatidae | 63% | 100% |
A0A3Q8IG58 | Leishmania donovani | 84% | 99% |
A0A422N5J3 | Trypanosoma rangeli | 50% | 100% |
A0A422NQE5 | Trypanosoma rangeli | 64% | 94% |
A1CL82 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 36% | 100% |
A1CQZ0 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 37% | 100% |
A1D3V4 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 37% | 100% |
A1D611 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 36% | 100% |
A2QU58 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 36% | 99% |
A2RB75 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 36% | 100% |
A3LSY7 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 37% | 100% |
A4IB59 | Leishmania infantum | 82% | 97% |
A4QTY2 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 35% | 100% |
A5D9W7 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 38% | 100% |
A5DZS4 | Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) | 38% | 97% |
A6R7B8 | Ajellomyces capsulatus (strain NAm1 / WU24) | 37% | 100% |
A6SDT7 | Botryotinia fuckeliana (strain B05.10) | 36% | 100% |
A6ZP43 | Saccharomyces cerevisiae (strain YJM789) | 36% | 100% |
A7F075 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 37% | 100% |
B0XPP3 | Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) | 38% | 100% |
B0Y081 | Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) | 36% | 100% |
C9ZQB0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
C9ZQB1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
C9ZZG8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 88% |
D0A1S2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
D0A6D7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AEY0 | Leishmania major | 83% | 99% |
E9B636 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 99% |
O74477 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 100% |
P0CM58 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 34% | 94% |
P0CM59 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 34% | 94% |
Q08601 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 36% | 100% |
Q0CQL9 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 36% | 100% |
Q0CTN3 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 36% | 100% |
Q1E0A3 | Coccidioides immitis (strain RS) | 38% | 94% |
Q2UCB7 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 36% | 100% |
Q2UN81 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 36% | 100% |
Q2VLK6 | Trypanosoma cruzi (strain CL Brener) | 47% | 100% |
Q2VLK8 | Trypanosoma cruzi (strain CL Brener) | 63% | 98% |
Q4PEQ5 | Ustilago maydis (strain 521 / FGSC 9021) | 39% | 100% |
Q4WJA1 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 38% | 100% |
Q4WYT0 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 36% | 100% |
Q585F3 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 48% | 100% |
Q5ANA8 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 36% | 97% |
Q6BH13 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 36% | 99% |
Q6C2Y6 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 36% | 94% |
Q6CLS0 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 37% | 100% |
Q6FPX9 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 35% | 100% |
Q75B43 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 36% | 96% |
Q7S232 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 36% | 96% |
Q7S4N5 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 37% | 100% |
Q7XJE6 | Arabidopsis thaliana | 32% | 100% |
Q8IEW1 | Trypanosoma brucei brucei | 55% | 87% |
Q8J140 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 37% | 100% |
Q8T8E5 | Trypanosoma brucei brucei | 40% | 100% |
Q8T8E6 | Trypanosoma brucei brucei | 49% | 100% |
Q8T8E7 | Trypanosoma brucei brucei | 48% | 100% |
V5BTK1 | Trypanosoma cruzi | 62% | 98% |