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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 6 |
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005802 | trans-Golgi network | 4 | 1 |
GO:0031984 | organelle subcompartment | 2 | 1 |
GO:0098791 | Golgi apparatus subcompartment | 3 | 1 |
Related structures:
AlphaFold database: A4HF64
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 7 |
GO:0006888 | endoplasmic reticulum to Golgi vesicle-mediated transport | 4 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016192 | vesicle-mediated transport | 4 | 7 |
GO:0046907 | intracellular transport | 3 | 7 |
GO:0048193 | Golgi vesicle transport | 5 | 7 |
GO:0051179 | localization | 1 | 7 |
GO:0051234 | establishment of localization | 2 | 7 |
GO:0051641 | cellular localization | 2 | 7 |
GO:0051649 | establishment of localization in cell | 3 | 7 |
GO:0006906 | vesicle fusion | 6 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007030 | Golgi organization | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016050 | vesicle organization | 5 | 1 |
GO:0048280 | vesicle fusion with Golgi apparatus | 6 | 1 |
GO:0048284 | organelle fusion | 5 | 1 |
GO:0061024 | membrane organization | 4 | 1 |
GO:0061025 | membrane fusion | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090174 | organelle membrane fusion | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.640 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.640 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.475 |
DEG_SPOP_SBC_1 | 40 | 44 | PF00917 | 0.630 |
DEG_SPOP_SBC_1 | 97 | 101 | PF00917 | 0.750 |
DOC_CDC14_PxL_1 | 436 | 444 | PF14671 | 0.312 |
DOC_CYCLIN_RxL_1 | 355 | 362 | PF00134 | 0.312 |
DOC_CYCLIN_yCln2_LP_2 | 321 | 327 | PF00134 | 0.312 |
DOC_MAPK_MEF2A_6 | 367 | 374 | PF00069 | 0.604 |
DOC_MAPK_MEF2A_6 | 403 | 412 | PF00069 | 0.278 |
DOC_MAPK_NFAT4_5 | 403 | 411 | PF00069 | 0.275 |
DOC_PIKK_1 | 282 | 290 | PF02985 | 0.615 |
DOC_PP1_RVXF_1 | 338 | 344 | PF00149 | 0.366 |
DOC_PP4_FxxP_1 | 277 | 280 | PF00568 | 0.616 |
DOC_PP4_FxxP_1 | 35 | 38 | PF00568 | 0.650 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.793 |
DOC_USP7_MATH_2 | 16 | 22 | PF00917 | 0.735 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.743 |
LIG_14-3-3_CanoR_1 | 151 | 156 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 39 | 48 | PF00244 | 0.682 |
LIG_Actin_WH2_2 | 388 | 405 | PF00022 | 0.486 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.703 |
LIG_BIR_III_4 | 212 | 216 | PF00653 | 0.631 |
LIG_CtBP_PxDLS_1 | 199 | 203 | PF00389 | 0.671 |
LIG_EH_1 | 305 | 309 | PF12763 | 0.603 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.312 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.396 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.711 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.695 |
LIG_GBD_Chelix_1 | 375 | 383 | PF00786 | 0.444 |
LIG_Integrin_RGD_1 | 367 | 369 | PF01839 | 0.324 |
LIG_LIR_Apic_2 | 11 | 16 | PF02991 | 0.697 |
LIG_LIR_Apic_2 | 154 | 158 | PF02991 | 0.640 |
LIG_LIR_Gen_1 | 432 | 443 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 446 | 454 | PF02991 | 0.388 |
LIG_LIR_LC3C_4 | 421 | 425 | PF02991 | 0.231 |
LIG_LIR_Nem_3 | 344 | 350 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 432 | 438 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 446 | 451 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 75 | 80 | PF02991 | 0.683 |
LIG_LYPXL_S_1 | 438 | 442 | PF13949 | 0.312 |
LIG_LYPXL_yS_3 | 439 | 442 | PF13949 | 0.312 |
LIG_MYND_3 | 284 | 288 | PF01753 | 0.610 |
LIG_NRBOX | 330 | 336 | PF00104 | 0.312 |
LIG_Pex14_2 | 444 | 448 | PF04695 | 0.312 |
LIG_PTAP_UEV_1 | 19 | 24 | PF05743 | 0.641 |
LIG_PTB_Apo_2 | 100 | 107 | PF02174 | 0.749 |
LIG_PTB_Phospho_1 | 100 | 106 | PF10480 | 0.749 |
LIG_REV1ctd_RIR_1 | 354 | 362 | PF16727 | 0.312 |
LIG_SH2_CRK | 155 | 159 | PF00017 | 0.646 |
LIG_SH2_CRK | 161 | 165 | PF00017 | 0.612 |
LIG_SH2_CRK | 381 | 385 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.711 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.690 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.682 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.660 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.673 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.587 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.598 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.640 |
LIG_SH3_3 | 434 | 440 | PF00018 | 0.312 |
LIG_SUMO_SIM_anti_2 | 330 | 336 | PF11976 | 0.352 |
LIG_SUMO_SIM_par_1 | 409 | 414 | PF11976 | 0.231 |
LIG_TRFH_1 | 381 | 385 | PF08558 | 0.312 |
LIG_TYR_ITIM | 379 | 384 | PF00017 | 0.312 |
LIG_TYR_ITIM | 437 | 442 | PF00017 | 0.312 |
LIG_UBA3_1 | 334 | 340 | PF00899 | 0.316 |
MOD_CDK_SPK_2 | 121 | 126 | PF00069 | 0.643 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.742 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.721 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.780 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.694 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.605 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.737 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.694 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.695 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.642 |
MOD_CMANNOS | 415 | 418 | PF00535 | 0.312 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.443 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.494 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.500 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.619 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.476 |
MOD_GlcNHglycan | 212 | 216 | PF01048 | 0.478 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.486 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.491 |
MOD_GlcNHglycan | 249 | 253 | PF01048 | 0.481 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.392 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.475 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.301 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.334 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.518 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.468 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.829 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.774 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.742 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.711 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.732 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.707 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.715 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.736 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.678 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.503 |
MOD_N-GLC_1 | 200 | 205 | PF02516 | 0.514 |
MOD_N-GLC_1 | 68 | 73 | PF02516 | 0.598 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.691 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.662 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.313 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.388 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.391 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.231 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.490 |
MOD_PKA_1 | 151 | 157 | PF00069 | 0.644 |
MOD_PKA_2 | 151 | 157 | PF00069 | 0.644 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.726 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.728 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.598 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.312 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.337 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.319 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.367 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.314 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.359 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.638 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.763 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.743 |
TRG_DiLeu_BaEn_1 | 432 | 437 | PF01217 | 0.475 |
TRG_DiLeu_BaLyEn_6 | 282 | 287 | PF01217 | 0.617 |
TRG_ENDOCYTIC_2 | 347 | 350 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 435 | 438 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 439 | 442 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 445 | 448 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.683 |
TRG_ER_diArg_1 | 294 | 296 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 55 | 57 | PF00400 | 0.758 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.788 |
TRG_Pf-PMV_PEXEL_1 | 126 | 130 | PF00026 | 0.436 |
TRG_Pf-PMV_PEXEL_1 | 295 | 299 | PF00026 | 0.372 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAG4 | Leptomonas seymouri | 57% | 81% |
A0A3S7X055 | Leishmania donovani | 78% | 85% |
A4I2E7 | Leishmania infantum | 79% | 85% |
E9AYK0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 85% |
Q4Q8X2 | Leishmania major | 79% | 85% |