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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HI97
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 7 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009451 | RNA modification | 5 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016070 | RNA metabolic process | 5 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
GO:0000154 | rRNA modification | 6 | 1 |
GO:0000455 | enzyme-directed rRNA pseudouridine synthesis | 8 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0031118 | rRNA pseudouridine synthesis | 7 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003723 | RNA binding | 4 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0009982 | pseudouridine synthase activity | 4 | 7 |
GO:0016853 | isomerase activity | 2 | 7 |
GO:0016866 | intramolecular transferase activity | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.335 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.346 |
CLV_PCSK_PC1ET2_1 | 288 | 290 | PF00082 | 0.418 |
CLV_PCSK_PC1ET2_1 | 407 | 409 | PF00082 | 0.542 |
CLV_PCSK_PC1ET2_1 | 49 | 51 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.346 |
DEG_COP1_1 | 210 | 218 | PF00400 | 0.442 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.430 |
DEG_ODPH_VHL_1 | 325 | 337 | PF01847 | 0.618 |
DEG_SPOP_SBC_1 | 152 | 156 | PF00917 | 0.442 |
DOC_CYCLIN_RxL_1 | 382 | 391 | PF00134 | 0.581 |
DOC_CYCLIN_yCln2_LP_2 | 177 | 183 | PF00134 | 0.442 |
DOC_MAPK_gen_1 | 278 | 287 | PF00069 | 0.589 |
DOC_MAPK_gen_1 | 331 | 337 | PF00069 | 0.546 |
DOC_MAPK_gen_1 | 405 | 415 | PF00069 | 0.613 |
DOC_MAPK_gen_1 | 48 | 56 | PF00069 | 0.600 |
DOC_MAPK_gen_1 | 87 | 96 | PF00069 | 0.531 |
DOC_MAPK_MEF2A_6 | 317 | 324 | PF00069 | 0.463 |
DOC_PP1_RVXF_1 | 338 | 345 | PF00149 | 0.585 |
DOC_PP1_RVXF_1 | 50 | 57 | PF00149 | 0.546 |
DOC_PP2B_LxvP_1 | 292 | 295 | PF13499 | 0.545 |
DOC_PP2B_LxvP_1 | 324 | 327 | PF13499 | 0.618 |
DOC_PP2B_LxvP_1 | 386 | 389 | PF13499 | 0.471 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.375 |
DOC_USP7_UBL2_3 | 194 | 198 | PF12436 | 0.442 |
DOC_USP7_UBL2_3 | 51 | 55 | PF12436 | 0.463 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.442 |
LIG_14-3-3_CanoR_1 | 200 | 205 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 207 | 216 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 278 | 287 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 317 | 323 | PF00244 | 0.442 |
LIG_BRCT_BRCA1_1 | 435 | 439 | PF00533 | 0.592 |
LIG_deltaCOP1_diTrp_1 | 428 | 433 | PF00928 | 0.509 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.589 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.546 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.544 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.618 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.413 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.593 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.546 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.483 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.582 |
LIG_FHA_2 | 261 | 267 | PF00498 | 0.546 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.483 |
LIG_LIR_Gen_1 | 25 | 36 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 369 | 379 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 428 | 437 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 236 | 242 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 369 | 374 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 428 | 433 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 436 | 442 | PF02991 | 0.509 |
LIG_NRBOX | 172 | 178 | PF00104 | 0.442 |
LIG_PCNA_PIPBox_1 | 86 | 95 | PF02747 | 0.618 |
LIG_SH2_CRK | 239 | 243 | PF00017 | 0.546 |
LIG_SH2_PTP2 | 93 | 96 | PF00017 | 0.546 |
LIG_SH2_SRC | 380 | 383 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.618 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.528 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.380 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.442 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.546 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.525 |
LIG_SUMO_SIM_anti_2 | 282 | 288 | PF11976 | 0.549 |
LIG_SUMO_SIM_anti_2 | 321 | 326 | PF11976 | 0.555 |
LIG_TYR_ITIM | 237 | 242 | PF00017 | 0.618 |
LIG_UBA3_1 | 284 | 288 | PF00899 | 0.546 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.585 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.514 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.618 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.536 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.515 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.695 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.508 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.515 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.456 |
MOD_CK2_1 | 260 | 266 | PF00069 | 0.546 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.493 |
MOD_CK2_1 | 423 | 429 | PF00069 | 0.731 |
MOD_Cter_Amidation | 329 | 332 | PF01082 | 0.346 |
MOD_GlcNHglycan | 115 | 119 | PF01048 | 0.346 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.355 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.242 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.542 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.721 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.352 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.346 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.592 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.510 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.420 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.754 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.595 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.710 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.358 |
MOD_N-GLC_1 | 419 | 424 | PF02516 | 0.588 |
MOD_N-GLC_2 | 137 | 139 | PF02516 | 0.418 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.515 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.571 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.389 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.552 |
MOD_OFUCOSY | 114 | 121 | PF10250 | 0.242 |
MOD_PIKK_1 | 306 | 312 | PF00454 | 0.442 |
MOD_PKA_1 | 409 | 415 | PF00069 | 0.503 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.565 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.503 |
MOD_Plk_1 | 419 | 425 | PF00069 | 0.629 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.576 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.592 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.546 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.546 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.367 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.442 |
TRG_DiLeu_BaEn_1 | 186 | 191 | PF01217 | 0.535 |
TRG_DiLeu_BaEn_2 | 428 | 434 | PF01217 | 0.501 |
TRG_DiLeu_BaEn_4 | 168 | 174 | PF01217 | 0.442 |
TRG_DiLeu_BaLyEn_6 | 382 | 387 | PF01217 | 0.449 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.504 |
TRG_ER_diArg_1 | 377 | 379 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 408 | 410 | PF00400 | 0.563 |
TRG_NLS_MonoCore_2 | 404 | 409 | PF00514 | 0.601 |
TRG_NLS_MonoCore_2 | 47 | 52 | PF00514 | 0.547 |
TRG_NLS_MonoExtC_3 | 404 | 409 | PF00514 | 0.601 |
TRG_NLS_MonoExtC_3 | 47 | 52 | PF00514 | 0.442 |
TRG_NLS_MonoExtN_4 | 405 | 410 | PF00514 | 0.605 |
TRG_NLS_MonoExtN_4 | 48 | 54 | PF00514 | 0.600 |
TRG_Pf-PMV_PEXEL_1 | 174 | 178 | PF00026 | 0.365 |
TRG_Pf-PMV_PEXEL_1 | 240 | 244 | PF00026 | 0.389 |
TRG_Pf-PMV_PEXEL_1 | 34 | 38 | PF00026 | 0.346 |
TRG_Pf-PMV_PEXEL_1 | 394 | 398 | PF00026 | 0.478 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P976 | Leptomonas seymouri | 50% | 100% |
A0A3S7X3F6 | Leishmania donovani | 72% | 100% |
A4I5I1 | Leishmania infantum | 72% | 100% |
E9B0S6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
Q4Q7F2 | Leishmania major | 71% | 100% |