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: Q4QCF5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.521 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.499 |
CLV_Separin_Metazoa | 11 | 15 | PF03568 | 0.591 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.496 |
DOC_CKS1_1 | 405 | 410 | PF01111 | 0.697 |
DOC_CKS1_1 | 439 | 444 | PF01111 | 0.543 |
DOC_MAPK_gen_1 | 8 | 15 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 89 | 98 | PF00069 | 0.529 |
DOC_MAPK_MEF2A_6 | 307 | 315 | PF00069 | 0.651 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.721 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.790 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.471 |
LIG_14-3-3_CanoR_1 | 155 | 163 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 248 | 253 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 52 | 61 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 91 | 96 | PF00244 | 0.535 |
LIG_deltaCOP1_diTrp_1 | 114 | 121 | PF00928 | 0.378 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.673 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.614 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.545 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.429 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.601 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.683 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.686 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.584 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.537 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.427 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.747 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.550 |
LIG_Integrin_isoDGR_2 | 82 | 84 | PF01839 | 0.647 |
LIG_LIR_Gen_1 | 269 | 277 | PF02991 | 0.631 |
LIG_LIR_Gen_1 | 421 | 431 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 133 | 138 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 269 | 274 | PF02991 | 0.644 |
LIG_LIR_Nem_3 | 421 | 426 | PF02991 | 0.621 |
LIG_NRBOX | 296 | 302 | PF00104 | 0.543 |
LIG_NRBOX | 357 | 363 | PF00104 | 0.508 |
LIG_PAM2_1 | 52 | 64 | PF00658 | 0.581 |
LIG_Pex14_1 | 139 | 143 | PF04695 | 0.523 |
LIG_Pex14_1 | 252 | 256 | PF04695 | 0.674 |
LIG_SH2_CRK | 143 | 147 | PF00017 | 0.524 |
LIG_SH2_PTP2 | 271 | 274 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.456 |
LIG_SH3_3 | 399 | 405 | PF00018 | 0.814 |
LIG_SH3_3 | 436 | 442 | PF00018 | 0.543 |
LIG_SUMO_SIM_anti_2 | 76 | 81 | PF11976 | 0.500 |
LIG_SUMO_SIM_par_1 | 158 | 164 | PF11976 | 0.450 |
LIG_SUMO_SIM_par_1 | 75 | 81 | PF11976 | 0.490 |
LIG_TRAF2_1 | 117 | 120 | PF00917 | 0.540 |
LIG_TRAF2_1 | 251 | 254 | PF00917 | 0.682 |
LIG_TYR_ITSM | 139 | 146 | PF00017 | 0.615 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.544 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.538 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.682 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.485 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.587 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.526 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.480 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.754 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.560 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.620 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.693 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.607 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.573 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.546 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.499 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.753 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.529 |
MOD_Cter_Amidation | 6 | 9 | PF01082 | 0.517 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.582 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.591 |
MOD_GlcNHglycan | 191 | 195 | PF01048 | 0.665 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.640 |
MOD_GlcNHglycan | 207 | 211 | PF01048 | 0.452 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.538 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.542 |
MOD_GlcNHglycan | 335 | 339 | PF01048 | 0.530 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.685 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.466 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.433 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.605 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.348 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.563 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.529 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.548 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.629 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.751 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.754 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.749 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.439 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.576 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.512 |
MOD_NEK2_2 | 309 | 314 | PF00069 | 0.541 |
MOD_NEK2_2 | 329 | 334 | PF00069 | 0.557 |
MOD_PIKK_1 | 106 | 112 | PF00454 | 0.532 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.742 |
MOD_PK_1 | 91 | 97 | PF00069 | 0.512 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.496 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.690 |
MOD_PKA_2 | 262 | 268 | PF00069 | 0.422 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.557 |
MOD_Plk_1 | 287 | 293 | PF00069 | 0.472 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.797 |
MOD_Plk_2-3 | 114 | 120 | PF00069 | 0.620 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.603 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.581 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.582 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.599 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.590 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.419 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.693 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.780 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.485 |
TRG_DiLeu_BaEn_1 | 11 | 16 | PF01217 | 0.587 |
TRG_DiLeu_BaEn_1 | 296 | 301 | PF01217 | 0.612 |
TRG_DiLeu_BaEn_1 | 353 | 358 | PF01217 | 0.515 |
TRG_DiLeu_BaLyEn_6 | 233 | 238 | PF01217 | 0.669 |
TRG_DiLeu_LyEn_5 | 11 | 16 | PF01217 | 0.587 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.595 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.636 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.438 |
TRG_ER_diArg_1 | 272 | 275 | PF00400 | 0.627 |
TRG_Pf-PMV_PEXEL_1 | 275 | 279 | PF00026 | 0.603 |
TRG_Pf-PMV_PEXEL_1 | 298 | 303 | PF00026 | 0.557 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM65 | Leptomonas seymouri | 38% | 74% |
A0A3S7WWF0 | Leishmania donovani | 93% | 84% |
A4HBQ7 | Leishmania braziliensis | 75% | 100% |
A4HZ59 | Leishmania infantum | 93% | 84% |
E9AV27 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |