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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HDG2
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016874 | ligase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 120 | 124 | PF00656 | 0.535 |
CLV_C14_Caspase3-7 | 200 | 204 | PF00656 | 0.555 |
CLV_C14_Caspase3-7 | 215 | 219 | PF00656 | 0.556 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.319 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 452 | 454 | PF00675 | 0.216 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.777 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.319 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 452 | 454 | PF00082 | 0.216 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.427 |
CLV_PCSK_PC1ET2_1 | 135 | 137 | PF00082 | 0.406 |
CLV_PCSK_PC1ET2_1 | 26 | 28 | PF00082 | 0.639 |
CLV_PCSK_PC1ET2_1 | 58 | 60 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.695 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.221 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.196 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.657 |
DEG_APCC_DBOX_1 | 32 | 40 | PF00400 | 0.634 |
DEG_APCC_DBOX_1 | 364 | 372 | PF00400 | 0.521 |
DEG_ODPH_VHL_1 | 360 | 371 | PF01847 | 0.514 |
DOC_CDC14_PxL_1 | 354 | 362 | PF14671 | 0.396 |
DOC_CDC14_PxL_1 | 478 | 486 | PF14671 | 0.521 |
DOC_MAPK_DCC_7 | 476 | 486 | PF00069 | 0.521 |
DOC_MAPK_gen_1 | 303 | 313 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 315 | 324 | PF00069 | 0.471 |
DOC_MAPK_gen_1 | 431 | 440 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 306 | 313 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 431 | 440 | PF00069 | 0.509 |
DOC_MAPK_NFAT4_5 | 306 | 314 | PF00069 | 0.454 |
DOC_PP2B_LxvP_1 | 314 | 317 | PF13499 | 0.498 |
DOC_PP2B_LxvP_1 | 4 | 7 | PF13499 | 0.664 |
DOC_PP4_FxxP_1 | 221 | 224 | PF00568 | 0.528 |
DOC_PP4_FxxP_1 | 479 | 482 | PF00568 | 0.521 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.493 |
DOC_USP7_UBL2_3 | 443 | 447 | PF12436 | 0.503 |
DOC_USP7_UBL2_3 | 58 | 62 | PF12436 | 0.510 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.514 |
LIG_14-3-3_CanoR_1 | 139 | 147 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 158 | 167 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 213 | 221 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 231 | 240 | PF00244 | 0.204 |
LIG_14-3-3_CanoR_1 | 452 | 456 | PF00244 | 0.408 |
LIG_APCC_ABBA_1 | 37 | 42 | PF00400 | 0.641 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.609 |
LIG_CaM_IQ_9 | 19 | 35 | PF13499 | 0.577 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.618 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.569 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.291 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.523 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.490 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.499 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.459 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.643 |
LIG_FHA_2 | 13 | 19 | PF00498 | 0.579 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.396 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.364 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.396 |
LIG_LIR_Apic_2 | 218 | 224 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 230 | 241 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 137 | 141 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 393 | 399 | PF02991 | 0.479 |
LIG_MYND_1 | 358 | 362 | PF01753 | 0.396 |
LIG_PDZ_Class_2 | 502 | 507 | PF00595 | 0.454 |
LIG_Pex14_2 | 333 | 337 | PF04695 | 0.521 |
LIG_SH2_GRB2like | 87 | 90 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.378 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.681 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.741 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.600 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.521 |
LIG_SH3_CIN85_PxpxPR_1 | 147 | 152 | PF14604 | 0.602 |
LIG_SUMO_SIM_anti_2 | 17 | 23 | PF11976 | 0.581 |
LIG_SUMO_SIM_anti_2 | 310 | 315 | PF11976 | 0.500 |
LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.639 |
LIG_TRAF2_1 | 269 | 272 | PF00917 | 0.396 |
LIG_TRFH_1 | 79 | 83 | PF08558 | 0.548 |
LIG_TYR_ITIM | 394 | 399 | PF00017 | 0.454 |
LIG_WRC_WIRS_1 | 258 | 263 | PF05994 | 0.521 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.667 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.557 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.571 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.504 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.636 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.396 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.378 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.396 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.396 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.474 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.482 |
MOD_Cter_Amidation | 47 | 50 | PF01082 | 0.728 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.711 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.745 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.220 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.308 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.320 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.588 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.693 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.510 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.338 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.444 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.417 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.533 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.524 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.596 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.523 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.507 |
MOD_N-GLC_1 | 185 | 190 | PF02516 | 0.500 |
MOD_N-GLC_1 | 249 | 254 | PF02516 | 0.321 |
MOD_N-GLC_1 | 495 | 500 | PF02516 | 0.196 |
MOD_N-GLC_1 | 88 | 93 | PF02516 | 0.574 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.547 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.611 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.396 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.541 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.399 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.521 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.454 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.509 |
MOD_PIKK_1 | 266 | 272 | PF00454 | 0.456 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.639 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.616 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.405 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.516 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.521 |
MOD_Plk_1 | 348 | 354 | PF00069 | 0.563 |
MOD_Plk_1 | 501 | 507 | PF00069 | 0.590 |
MOD_Plk_2-3 | 177 | 183 | PF00069 | 0.516 |
MOD_Plk_2-3 | 456 | 462 | PF00069 | 0.396 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.586 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.488 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.521 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.454 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.438 |
MOD_Plk_4 | 495 | 501 | PF00069 | 0.509 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.646 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.519 |
MOD_SUMO_for_1 | 103 | 106 | PF00179 | 0.533 |
MOD_SUMO_for_1 | 57 | 60 | PF00179 | 0.508 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.454 |
TRG_ER_diArg_1 | 317 | 319 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 433 | 435 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 49 | 51 | PF00400 | 0.761 |
TRG_Pf-PMV_PEXEL_1 | 413 | 417 | PF00026 | 0.286 |
TRG_Pf-PMV_PEXEL_1 | 476 | 480 | PF00026 | 0.196 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5X3 | Leptomonas seymouri | 57% | 100% |
A0A1X0NQT7 | Trypanosomatidae | 26% | 100% |
A0A3S7WYE0 | Leishmania donovani | 77% | 85% |
A4I0U3 | Leishmania infantum | 78% | 85% |
C9ZVE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9AWU7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4QAM7 | Leishmania major | 77% | 100% |