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 | yes | yes: 1, no: 6 |
NetGPI | no | yes: 0, no: 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 245 | 249 | PF00656 | 0.575 |
CLV_C14_Caspase3-7 | 284 | 288 | PF00656 | 0.512 |
CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.738 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.576 |
CLV_PCSK_FUR_1 | 102 | 106 | PF00082 | 0.744 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.734 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.546 |
DEG_APCC_DBOX_1 | 12 | 20 | PF00400 | 0.450 |
DEG_SPOP_SBC_1 | 109 | 113 | PF00917 | 0.626 |
DOC_CDC14_PxL_1 | 364 | 372 | PF14671 | 0.503 |
DOC_CYCLIN_RxL_1 | 259 | 269 | PF00134 | 0.574 |
DOC_MAPK_gen_1 | 11 | 18 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 252 | 262 | PF00069 | 0.554 |
DOC_MAPK_MEF2A_6 | 206 | 215 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 265 | 272 | PF00069 | 0.440 |
DOC_PP4_FxxP_1 | 22 | 25 | PF00568 | 0.454 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.448 |
DOC_USP7_UBL2_3 | 379 | 383 | PF12436 | 0.361 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.403 |
LIG_14-3-3_CanoR_1 | 132 | 136 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 71 | 80 | PF00244 | 0.623 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.472 |
LIG_CtBP_PxDLS_1 | 140 | 144 | PF00389 | 0.632 |
LIG_eIF4E_1 | 169 | 175 | PF01652 | 0.463 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.720 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.476 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.535 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.617 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.518 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.433 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.725 |
LIG_LIR_Apic_2 | 134 | 140 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 12 | 23 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 255 | 264 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 374 | 385 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 134 | 139 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 255 | 260 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.537 |
LIG_NRBOX | 15 | 21 | PF00104 | 0.451 |
LIG_PCNA_TLS_4 | 265 | 272 | PF02747 | 0.493 |
LIG_Pex14_2 | 18 | 22 | PF04695 | 0.450 |
LIG_SH2_CRK | 257 | 261 | PF00017 | 0.508 |
LIG_SH2_SRC | 271 | 274 | PF00017 | 0.613 |
LIG_SH2_STAT3 | 295 | 298 | PF00017 | 0.553 |
LIG_SH2_STAT3 | 315 | 318 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.530 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.450 |
LIG_SUMO_SIM_par_1 | 48 | 54 | PF11976 | 0.476 |
LIG_TRAF2_1 | 273 | 276 | PF00917 | 0.566 |
LIG_TRAF2_1 | 325 | 328 | PF00917 | 0.538 |
LIG_TRFH_1 | 169 | 173 | PF08558 | 0.454 |
LIG_TYR_ITIM | 362 | 367 | PF00017 | 0.465 |
MOD_CDK_SPK_2 | 233 | 238 | PF00069 | 0.507 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.542 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.418 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.667 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.496 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.607 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.446 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.499 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.488 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.738 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.670 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.681 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.589 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.742 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.648 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.462 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.593 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.696 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.609 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.480 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.524 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.459 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.740 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.585 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.569 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.538 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.595 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.627 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.686 |
MOD_LATS_1 | 336 | 342 | PF00433 | 0.523 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.448 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.447 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.581 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.406 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.679 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.739 |
MOD_NEK2_2 | 6 | 11 | PF00069 | 0.449 |
MOD_NEK2_2 | 64 | 69 | PF00069 | 0.654 |
MOD_PIKK_1 | 399 | 405 | PF00454 | 0.429 |
MOD_PKA_1 | 252 | 258 | PF00069 | 0.533 |
MOD_PKA_1 | 399 | 405 | PF00069 | 0.429 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.552 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.571 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.595 |
MOD_PKA_2 | 395 | 401 | PF00069 | 0.552 |
MOD_PKB_1 | 69 | 77 | PF00069 | 0.529 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.481 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.597 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.550 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.481 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.455 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.511 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.415 |
MOD_SUMO_rev_2 | 344 | 351 | PF00179 | 0.467 |
TRG_DiLeu_BaEn_1 | 216 | 221 | PF01217 | 0.581 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 364 | 367 | PF00928 | 0.464 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 102 | 105 | PF00400 | 0.725 |
TRG_ER_diArg_1 | 251 | 253 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 68 | 71 | PF00400 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 164 | 168 | PF00026 | 0.516 |
TRG_Pf-PMV_PEXEL_1 | 265 | 269 | PF00026 | 0.439 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCF7 | Leptomonas seymouri | 58% | 100% |
A0A1X0NWV8 | Trypanosomatidae | 34% | 100% |
A0A3S7WYC1 | Leishmania donovani | 75% | 100% |
A4I0S5 | Leishmania infantum | 75% | 100% |
E9AWS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4QAP7 | Leishmania major | 74% | 100% |